Publications of Huntington F Willard     :chronological  combined  bibtex listing:

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Papers Published

  1. J Basu, G Stromberg, G Compitello, HF Willard, G Van Bokkelen, Rapid creation of BAC-based human artificial chromosome vectors by transposition with synthetic alpha-satellite arrays., Nucleic acids research, England, vol. 33 no. 2 (2005), pp. 587-96  [abs].
  2. BP Chadwick, HF Willard, Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome., Proceedings of the National Academy of Sciences of the United States of America, United States, vol. 101 no. 50 (December, 2004), pp. 17450-5  [abs].
  3. MK Rudd, HF Willard, Analysis of the centromeric regions of the human genome assembly., Trends in genetics : TIG, England, vol. 20 no. 11 (November, 2004), pp. 529-33  [abs].
  4. BR Grimes, J Babcock, MK Rudd, B Chadwick, HF Willard, Assembly and characterization of heterochromatin and euchromatin on human artificial chromosomes., Genome biology, England, vol. 5 no. 11 (2004), pp. R89  [abs].
  5. BP Chadwick, HF Willard, Barring gene expression after XIST: maintaining facultative heterochromatin on the inactive X., Seminars in cell & developmental biology, England, vol. 14 no. 6 (December, 2003), pp. 359-67  [abs].
  6. MK Rudd, RW Mays, S Schwartz, HF Willard, Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag., Molecular and cellular biology, United States, vol. 23 no. 21 (November, 2003), pp. 7689-97  [abs].
  7. BP Chadwick, HF Willard, Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome., Human molecular genetics, England, vol. 12 no. 17 (September, 2003), pp. 2167-78  [abs].
  8. I Percec, JL Thorvaldsen, RM Plenge, CJ Krapp, JH Nadeau, HF Willard, MS Bartolomei, An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse., Genetics, United States, vol. 164 no. 4 (August, 2003), pp. 1481-94  [abs].
  9. HF Willard, Tales of the Y chromosome., Nature, England, vol. 423 no. 6942 (June, 2003), pp. 810-1, 813 .
  10. BP Chadwick, HF Willard, SETting the stage. Eed-Enx1 leaves an epigenetic signature on the inactive X chromosome., Developmental cell, United States, vol. 4 no. 4 (April, 2003), pp. 445-7  [abs].
  11. RS Williams, HF Willard, R Snyderman, Personalized health planning., Science (New York, N.Y.), United States, vol. 300 no. 5619 (April, 2003), pp. 549 .
  12. MK Rudd, MG Schueler, HF Willard, Sequence organization and functional annotation of human centromeres., Cold Spring Harbor symposia on quantitative biology, United States, vol. 68 (2003), pp. 141-9 .
  13. RM Plenge, RA Stevenson, HA Lubs, CE Schwartz, HF Willard, Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders., American journal of human genetics, United States, vol. 71 no. 1 (July, 2002), pp. 168-73  [abs].
  14. BR Grimes, AA Rhoades, HF Willard, Alpha-satellite DNA and vector composition influence rates of human artificial chromosome formation., Molecular therapy : the journal of the American Society of Gene Therapy, United States, vol. 5 no. 6 (June, 2002), pp. 798-805  [abs].
  15. LL Hall, M Byron, K Sakai, L Carrel, HF Willard, JB Lawrence, An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells., Proceedings of the National Academy of Sciences of the United States of America, United States, vol. 99 no. 13 (June, 2002), pp. 8677-82  [abs].
  16. BP Chadwick, HF Willard, Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome., The Journal of cell biology, United States, vol. 157 no. 7 (June, 2002), pp. 1113-23  [abs].
  17. I Percec, RM Plenge, JH Nadeau, MS Bartolomei, HF Willard, Autosomal dominant mutations affecting X inactivation choice in the mouse., Science (New York, N.Y.), United States, vol. 296 no. 5570 (May, 2002), pp. 1136-9  [abs].
  18. HF Willard, 2001 ASHG Presidential Address. On black boxes and storytellers: lessons learned in human genetics., American journal of human genetics, United States, vol. 70 no. 2 (February, 2002), pp. 285-96 .
  19. HF Willard, You say tomato and I say tomahto: human genetics and gene therapy., Molecular therapy : the journal of the American Society of Gene Therapy, United States, vol. 4 no. 6 (December, 2001), pp. 514 .
  20. MG Schueler, AW Higgins, MK Rudd, K Gustashaw, HF Willard, Genomic and genetic definition of a functional human centromere., Science (New York, N.Y.), United States, vol. 294 no. 5540 (October, 2001), pp. 109-15  [abs].
  21. HF Willard, L Carrel, Making sense (and antisense) of the X inactivation center., Proceedings of the National Academy of Sciences of the United States of America, United States, vol. 98 no. 18 (August, 2001), pp. 10025-7 .
  22. BP Chadwick, CM Valley, HF Willard, Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome., Nucleic acids research, England, vol. 29 no. 13 (July, 2001), pp. 2699-705  [abs].
  23. BP Chadwick, HF Willard, Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant., Human molecular genetics, England, vol. 10 no. 10 (May, 2001), pp. 1101-13  [abs].
  24. HF Willard, Neocentromeres and human artificial chromosomes: an unnatural act., Proceedings of the National Academy of Sciences of the United States of America, United States, vol. 98 no. 10 (May, 2001), pp. 5374-6 .
  25. BP Chadwick, HF Willard, A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosome., The Journal of cell biology, United States, vol. 152 no. 2 (January, 2001), pp. 375-84  [abs].
  26. HF Willard, Genomics and gene therapy. Artificial chromosomes coming to life., Science (New York, N.Y.), UNITED STATES, vol. 290 no. 5495 (November, 2000), pp. 1308-9  [abs].
  27. KD Tsuchiya, HF Willard, Chromosomal domains and escape from X inactivation: comparative X inactivation analysis in mouse and human., Mammalian genome : official journal of the International Mammalian Genome Society, UNITED STATES, vol. 11 no. 10 (October, 2000), pp. 849-54  [abs].
  28. RM Plenge, I Percec, JH Nadeau, HF Willard, Expression-based assay of an X-linked gene to examine effects of the X-controlling element (Xce) locus., Mammalian genome : official journal of the International Mammalian Genome Society, UNITED STATES, vol. 11 no. 5 (May, 2000), pp. 405-8 .
  29. MG Schueler, AW Higgins, R Nagaraja, D Tentler, N Dahl, K Gustashaw, HF Willard, Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patients with androgen insensitivity and mental retardation., Genomics, UNITED STATES, vol. 66 no. 1 (May, 2000), pp. 104-9  [abs].
  30. M Thibonnier, MK Graves, MS Wagner, N Chatelain, F Soubrier, P Corvol, HF Willard, X Jeunemaitre, Study of V(1)-vascular vasopressin receptor gene microsatellite polymorphisms in human essential hypertension., Journal of molecular and cellular cardiology, ENGLAND, vol. 32 no. 4 (April, 2000), pp. 557-64  [abs].
  31. L Carrel, AA Cottle, KC Goglin, HF Willard, A first-generation X-inactivation profile of the human X chromosome., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 96 no. 25 (December, 1999), pp. 14440-4  [abs].
  32. HF Willard, BD Hendrich, Breaking the silence in Rett syndrome., Nature genetics, UNITED STATES, vol. 23 no. 2 (October, 1999), pp. 127-8 .
  33. AW Higgins, MG Schueler, HF Willard, Chromosome engineering: generation of mono- and dicentric isochromosomes in a somatic cell hybrid system., Chromosoma, GERMANY, vol. 108 no. 4 (August, 1999), pp. 256-65  [abs].
  34. D Tentler, P Gustavsson, J Leisti, M Schueler, J Chelly, E Timonen, G Annerén, HF Willard, N Dahl, Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia., European journal of human genetics : EJHG, ENGLAND, vol. 7 no. 5 (July, 1999), pp. 541-8  [abs].
  35. L Carrel, HF Willard, Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 96 no. 13 (June, 1999), pp. 7364-9  [abs].
  36. RM Plenge, L Tranebjaerg, PK Jensen, C Schwartz, HF Willard, Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation., American journal of human genetics, UNITED STATES, vol. 64 no. 3 (March, 1999), pp. 759-67  [abs].
  37. BA Sullivan, HF Willard, Stable dicentric X chromosomes with two functional centromeres., Nature genetics, UNITED STATES, vol. 20 no. 3 (November, 1998), pp. 227-8 .
  38. L Carrel, HF Willard, Counting on Xist., Nature genetics, UNITED STATES, vol. 19 no. 3 (July, 1998), pp. 211-2 .
  39. AP Miller, HF Willard, Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 95 no. 15 (July, 1998), pp. 8709-14  [abs].
  40. WM White, HF Willard, DL Van Dyke, DJ Wolff, The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA., American journal of human genetics, UNITED STATES, vol. 63 no. 1 (July, 1998), pp. 20-8  [abs].
  41. HF Willard, KE Davies, Genetics of disease Complex genetics, complex diseases, Curr Opin Genet Dev, vol. 8 no. 3 (June, 1998), pp. 271-3 .
  42. T Haaf, HF Willard, Orangutan alpha-satellite monomers are closely related to the human consensus sequence., Mammalian genome : official journal of the International Mammalian Genome Society, UNITED STATES, vol. 9 no. 6 (June, 1998), pp. 440-7  [abs].
  43. HF Willard, Human artificial chromosomes coming into focus., Nature biotechnology, UNITED STATES, vol. 16 no. 5 (May, 1998), pp. 415-6 .
  44. HF Willard, Centromeres: the missing link in the development of human artificial chromosomes., Current opinion in genetics & development, ENGLAND, vol. 8 no. 2 (April, 1998), pp. 219-25  [abs].
  45. A Greenfield, L Carrel, D Pennisi, C Philippe, N Quaderi, P Siggers, K Steiner, PP Tam, AP Monaco, HF Willard, P Koopman, The UTX gene escapes X inactivation in mice and humans., Human molecular genetics, ENGLAND, vol. 7 no. 4 (April, 1998), pp. 737-42  [abs].
  46. L Dal Zotto, NA Quaderi, R Elliott, PA Lingerfelter, L Carrel, V Valsecchi, E Montini, CH Yen, V Chapman, I Kalcheva, G Arrigo, O Zuffardi, S Thomas, HF Willard, A Ballabio, CM Disteche, EI Rugarli, The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region., Human molecular genetics, ENGLAND, vol. 7 no. 3 (March, 1998), pp. 489-99  [abs].
  47. MM Mahtani, HF Willard, Physical and genetic mapping of the human X chromosome centromere: repression of recombination., Genome research, UNITED STATES, vol. 8 no. 2 (February, 1998), pp. 100-10  [abs].
  48. JM Puck, HF Willard, X inactivation in females with X-linked disease., The New England journal of medicine, UNITED STATES, vol. 338 no. 5 (January, 1998), pp. 325-8 .
  49. RM Plenge, BD Hendrich, C Schwartz, JF Arena, A Naumova, C Sapienza, RM Winter, HF Willard, A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation., Nature genetics, UNITED STATES, vol. 17 no. 3 (November, 1997), pp. 353-6  [abs].
  50. RS James, P Dalton, K Gustashaw, DJ Wolff, HF Willard, C Mitchell, PA Jacobs, Molecular characterization of isochromosomes of Xq., Annals of human genetics, ENGLAND, vol. 61 no. Pt 6 (November, 1997), pp. 485-90  [abs].
  51. T Haaf, HF Willard, Chromosome-specific alpha-satellite DNA from the centromere of chimpanzee chromosome 4., Chromosoma, GERMANY, vol. 106 no. 4 (September, 1997), pp. 226-32  [abs].
  52. Y Ishikawa-Brush, JF Powell, P Bolton, AP Miller, F Francis, HF Willard, H Lehrach, AP Monaco, Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene., Human molecular genetics, ENGLAND, vol. 6 no. 8 (August, 1997), pp. 1241-50  [abs].
  53. DJ Wolff, KM Gustashaw, V Zurcher, L Ko, W White, L Weiss, DL Van Dyke, S Schwartz, HF Willard, Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern., Human genetics, GERMANY, vol. 100 no. 2 (August, 1997), pp. 256-61  [abs].
  54. TW Depinet, JL Zackowski, WC Earnshaw, S Kaffe, GS Sekhon, R Stallard, BA Sullivan, GH Vance, DL Van Dyke, HF Willard, AB Zinn, S Schwartz, Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA., Human molecular genetics, ENGLAND, vol. 6 no. 8 (August, 1997), pp. 1195-204  [abs].
  55. BD Hendrich, RM Plenge, HF Willard, Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation., Nucleic acids research, ENGLAND, vol. 25 no. 13 (July, 1997), pp. 2661-71  [abs].
  56. CJ Brown, L Carrel, HF Willard, Expression of genes from the human active and inactive X chromosomes., American journal of human genetics, UNITED STATES, vol. 60 no. 6 (June, 1997), pp. 1333-43  [abs].
  57. JJ Harrington, G Van Bokkelen, RW Mays, K Gustashaw, HF Willard, Formation of de novo centromeres and construction of first-generation human artificial microchromosomes., Nature genetics, UNITED STATES, vol. 15 no. 4 (April, 1997), pp. 345-55  [abs].
  58. HF Willard, HK Salz, Remodelling chromatin with RNA., Nature, ENGLAND, vol. 386 no. 6622 (March, 1997), pp. 228-9 .
  59. L Carrel, PA Hunt, HF Willard, Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene., Human molecular genetics, ENGLAND, vol. 5 no. 9 (September, 1996), pp. 1361-6  [abs].
  60. HF Willard, Chromosome manipulation: a systematic approach toward understanding human chromosome structure and function., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 93 no. 14 (July, 1996), pp. 6847-50 .
  61. HF Willard, X chromosome inactivation and X-linked mental retardation., American journal of medical genetics, UNITED STATES, vol. 64 no. 1 (July, 1996), pp. 21-6  [abs].
  62. L Carrel, HF Willard, An assay for X inactivation based on differential methylation at the fragile X locus, FMR1., American journal of medical genetics, UNITED STATES, vol. 64 no. 1 (July, 1996), pp. 27-30  [abs].
  63. HF Willard, X chromosome inactivation, XIST, and pursuit of the X-inactivation center., Cell, UNITED STATES, vol. 86 no. 1 (July, 1996), pp. 5-7 .
  64. AK Naumova, RM Plenge, LM Bird, M Leppert, K Morgan, HF Willard, C Sapienza, Heritability of X chromosome--inactivation phenotype in a large family., American journal of human genetics, UNITED STATES, vol. 58 no. 6 (June, 1996), pp. 1111-9  [abs].
  65. PE Warburton, T Haaf, J Gosden, D Lawson, HF Willard, Characterization of a chromosome-specific chimpanzee alpha satellite subset: evolutionary relationship to subsets on human chromosomes., Genomics, UNITED STATES, vol. 33 no. 2 (April, 1996), pp. 220-8  [abs].
  66. L Carrel, CM Clemson, JM Dunn, AP Miller, PA Hunt, JB Lawrence, HF Willard, X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse., Human molecular genetics, ENGLAND, vol. 5 no. 3 (March, 1996), pp. 391-401  [abs].
  67. CM Clemson, JA McNeil, HF Willard, JB Lawrence, XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure., The Journal of cell biology, UNITED STATES, vol. 132 no. 3 (February, 1996), pp. 259-75  [abs].
  68. M Thibonnier, MK Graves, MS Wagner, C Auzan, E Clauser, HF Willard, Structure, sequence, expression, and chromosomal localization of the human V1a vasopressin receptor gene., Genomics, UNITED STATES, vol. 31 no. 3 (February, 1996), pp. 327-34  [abs].
  69. MP Coleman, HJ Ambrose, L Carrel, AH Németh, HF Willard, KE Davies, A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status., Genomics, UNITED STATES, vol. 31 no. 1 (January, 1996), pp. 135-8  [abs].
  70. DJ Wolff, AP Miller, DL Van Dyke, S Schwartz, HF Willard, Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation., American journal of human genetics, UNITED STATES, vol. 58 no. 1 (January, 1996), pp. 154-60  [abs].
  71. BA Sullivan, S Schwartz, HF Willard, Centromeres of human chromosomes., Environmental and molecular mutagenesis, UNITED STATES, vol. 28 no. 3 (1996), pp. 182-91  [abs].
  72. CU Kirchgessner, ST Warren, HF Willard, X inactivation of the FMR1 fragile X mental retardation gene., Journal of medical genetics, ENGLAND, vol. 32 no. 12 (December, 1995), pp. 925-9  [abs].
  73. PE Warburton, HF Willard, Interhomologue sequence variation of alpha satellite DNA from human chromosome 17: evidence for concerted evolution along haplotypic lineages., Journal of molecular evolution, UNITED STATES, vol. 41 no. 6 (December, 1995), pp. 1006-15  [abs].
  74. R Sultana, DA Adler, S Edelhoff, L Carrel, KH Lee, VC Chapman, HF Willard, CM Disteche, The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation., Human molecular genetics, ENGLAND, vol. 4 no. 2 (February, 1995), pp. 257-63  [abs].
  75. T Alitalo, F Francis, J Kere, H Lehrach, D Schlessinger, HF Willard, A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes., Genomics, UNITED STATES, vol. 25 no. 3 (February, 1995), pp. 691-700  [abs].
  76. CJ Brown, AP Miller, L Carrel, JL Rupert, KE Davies, HF Willard, The DXS423E gene in Xp11.21 escapes X chromosome inactivation., Human molecular genetics, ENGLAND, vol. 4 no. 2 (February, 1995), pp. 251-5  [abs].
  77. BD Hendrich, HF Willard, Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals., Human molecular genetics, ENGLAND, vol. 4 Spec No (1995), pp. 1765-77  [abs].
  78. JL Rupert, CJ Brown, HF Willard, Direct detection of non-random X chromosome inactivation by use of a transcribed polymorphism in the XIST gene., European journal of human genetics : EJHG, SWITZERLAND, vol. 3 no. 6 (1995), pp. 333-43  [abs].
  79. KM Gustashaw, V Zurcher, LH Dickerman, R Stallard, HF Willard, Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation., American journal of medical genetics, UNITED STATES, vol. 53 no. 1 (October, 1994), pp. 39-45  [abs].
  80. RG Lafrenière, L Carrel, HF Willard, A novel transmembrane transporter encoded by the XPCT gene in Xq13.2., Human molecular genetics, ENGLAND, vol. 3 no. 7 (July, 1994), pp. 1133-9  [abs].
  81. KA Rack, J Chelly, RJ Gibbons, S Rider, D Benjamin, RG Lafreniére, D Oscier, RW Hendriks, IW Craig, HF Willard, Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia., Human molecular genetics, ENGLAND, vol. 3 no. 7 (July, 1994), pp. 1053-9  [abs].
  82. DJ Wolff, CJ Brown, S Schwartz, AM Duncan, U Surti, HF Willard, Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations., American journal of human genetics, UNITED STATES, vol. 55 no. 1 (July, 1994), pp. 87-95  [abs].
  83. V Reed, SH Laval, V McCabe, HF Willard, Y Boyd, Mapping of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse., Mammalian genome : official journal of the International Mammalian Genome Society, UNITED STATES, vol. 5 no. 4 (April, 1994), pp. 237-40 .
  84. CJ Brown, HF Willard, The human X-inactivation centre is not required for maintenance of X-chromosome inactivation., Nature, ENGLAND, vol. 368 no. 6467 (March, 1994), pp. 154-6  [abs].
  85. HF Willard, F Cremers, JL Mandel, AP Monaco, DL Nelson, D Schlessinger, Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994., Cytogenetics and cell genetics, SWITZERLAND, vol. 67 no. 4 (1994), pp. 295-358 .
  86. AM Duncan, A Macdonald, CJ Brown, D Wolff, HF Willard, B Sutton, Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization., American journal of medical genetics, UNITED STATES, vol. 47 no. 8 (December, 1993), pp. 1153-6  [abs].
  87. GM Greig, PE Warburton, HF Willard, Organization and evolution of an alpha satellite DNA subset shared by human chromosomes 13 and 21., Journal of molecular evolution, UNITED STATES, vol. 37 no. 5 (November, 1993), pp. 464-75  [abs].
  88. GM Greig, CB Sharp, L Carrel, HF Willard, Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies., Human molecular genetics, ENGLAND, vol. 2 no. 10 (October, 1993), pp. 1611-8  [abs].
  89. PE Warburton, JS Waye, HF Willard, Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin., Molecular and cellular biology, UNITED STATES, vol. 13 no. 10 (October, 1993), pp. 6520-9  [abs].
  90. HF Willard, The inv(16) in acute nonlymphocytic leukemia: a turnabout for myosin heavy chain., Human molecular genetics, ENGLAND, vol. 2 no. 10 (October, 1993), pp. 1525-6 .
  91. RG Lafrenière, HF Willard, Pulsed-field map of Xq13 in the region of the human X inactivation center., Genomics, UNITED STATES, vol. 17 no. 2 (August, 1993), pp. 502-6  [abs].
  92. JM Puck, SM Deschênes, JC Porter, AS Dutra, CJ Brown, HF Willard, PS Henthorn, The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1., Human molecular genetics, ENGLAND, vol. 2 no. 8 (August, 1993), pp. 1099-104  [abs].
  93. RG Lafrenière, CJ Brown, S Rider, J Chelly, P Taillon-Miller, AC Chinault, AP Monaco, HF Willard, 2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes., Human molecular genetics, ENGLAND, vol. 2 no. 8 (August, 1993), pp. 1105-15  [abs].
  94. KA Leppig, CJ Brown, SL Bressler, K Gustashaw, RA Pagon, HF Willard, CM Disteche, Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST., Human molecular genetics, ENGLAND, vol. 2 no. 7 (July, 1993), pp. 883-7  [abs].
  95. BD Hendrich, CJ Brown, HF Willard, Evolutionary conservation of possible functional domains of the human and murine XIST genes., Human molecular genetics, ENGLAND, vol. 2 no. 6 (June, 1993), pp. 663-72  [abs].
  96. C Tyler-Smith, HF Willard, Mammalian chromosome structure., Current opinion in genetics & development, ENGLAND, vol. 3 no. 3 (June, 1993), pp. 390-7  [abs].
  97. T Haaf, M Schmid, C Steinlein, PM Galetti, HF Willard, Organization and molecular cytogenetics of a satellite DNA family from Hoplias malabaricus (Pisces, Erythrinidae)., Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology, ENGLAND, vol. 1 no. 1 (May, 1993), pp. 77-86  [abs].
  98. HF Willard, The needle found!!! Trinucleotide repeat expansion in the Huntington's disease gene., Human molecular genetics, ENGLAND, vol. 2 no. 5 (May, 1993), pp. 497-8 .
  99. MM Mahtani, HF Willard, A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat loci., Human molecular genetics, ENGLAND, vol. 2 no. 4 (April, 1993), pp. 431-7  [abs].
  100. HF Willard, Cloning of the X-linked glycerol kinase gene., Human molecular genetics, ENGLAND, vol. 2 no. 2 (February, 1993), pp. 95-6 .
  101. HF Willard, CJ Brown, L Carrel, B Hendrich, AP Miller, Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation., Cold Spring Harbor symposia on quantitative biology, UNITED STATES, vol. 58 (1993), pp. 315-22 .
  102. D Schlessinger, JL Mandel, AP Monaco, DL Nelson, HF Willard, Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993., Cytogenetics and cell genetics, SWITZERLAND, vol. 64 no. 3-4 (1993), pp. 147-94 .
  103. R Wevrick, VP Willard, HF Willard, Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7., Genomics, UNITED STATES, vol. 14 no. 4 (December, 1992), pp. 912-23  [abs].
  104. BJ Lorber, M Grantham, J Peters, HF Willard, TJ Hassold, Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin., American journal of human genetics, UNITED STATES, vol. 51 no. 6 (December, 1992), pp. 1265-76  [abs].
  105. HF Willard, Centromeres--primary constrictions are primarily complicated., Human molecular genetics, ENGLAND, vol. 1 no. 9 (December, 1992), pp. 667-8 .
  106. PE Warburton, HF Willard, PCR amplification of tandemly repeated DNA: analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA., Nucleic acids research, ENGLAND, vol. 20 no. 22 (November, 1992), pp. 6033-42  [abs].
  107. RA Bascom, J García-Heras, CL Hsieh, DS Gerhard, C Jones, U Francke, HF Willard, DH Ledbetter, RR McInnes, Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM., American journal of human genetics, UNITED STATES, vol. 51 no. 5 (November, 1992), pp. 1028-35  [abs].
  108. CJ Brown, BD Hendrich, JL Rupert, RG Lafrenière, Y Xing, J Lawrence, HF Willard, The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus., Cell, UNITED STATES, vol. 71 no. 3 (October, 1992), pp. 527-42  [abs].
  109. JL Mandel, AP Monaco, DL Nelson, D Schlessinger, HF Willard, M Chipperfield, P Pearson, P Gilna, M Cinkosky, Genome maps III. 1992. Wall Chart., Science (New York, N.Y.), UNITED STATES, vol. 258 no. 5079 (October, 1992), pp. 87-102 .
  110. T Haaf, PE Warburton, HF Willard, Integration of human alpha-satellite DNA into simian chromosomes: centromere protein binding and disruption of normal chromosome segregation., Cell, UNITED STATES, vol. 70 no. 4 (August, 1992), pp. 681-96  [abs].
  111. IA Corcos, RG Lafrenière, CR Begy, R Loch-Caruso, HF Willard, TW Glover, Refined localization of human connexin32 gene locus, GJB1, to Xq13.1., Genomics, UNITED STATES, vol. 13 no. 2 (June, 1992), pp. 479-80  [abs].
  112. A Ballabio, HF Willard, Mammalian X-chromosome inactivation and the XIST gene., Current opinion in genetics & development, ENGLAND, vol. 2 no. 3 (June, 1992), pp. 439-47  [abs].
  113. T Haaf, HF Willard, Organization, polymorphism, and molecular cytogenetics of chromosome-specific alpha-satellite DNA from the centromere of chromosome 2., Genomics, UNITED STATES, vol. 13 no. 1 (May, 1992), pp. 122-8  [abs].
  114. PD Cotter, HF Willard, JL Gorski, DF Bishop, Assignment of human erythroid delta-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.21 by PCR analysis of somatic cell hybrids containing X; autosome translocations., Genomics, UNITED STATES, vol. 13 no. 1 (May, 1992), pp. 211-2  [abs].
  115. CA Quigley, KJ Friedman, A Johnson, RG Lafreniere, LM Silverman, DB Lubahn, TR Brown, EM Wilson, HF Willard, FS French, Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status., The Journal of clinical endocrinology and metabolism, UNITED STATES, vol. 74 no. 4 (April, 1992), pp. 927-33  [abs].
  116. GM Greig, HF Willard, Beta satellite DNA: characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes., Genomics, UNITED STATES, vol. 12 no. 3 (March, 1992), pp. 573-80  [abs].
  117. T Haaf, AT Sumner, J Köhler, HF Willard, M Schmid, AT Summer, A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma., Cytogenetics and cell genetics, SWITZERLAND, vol. 60 no. 1 (1992), pp. 12-7  [abs].
  118. MP Coleman, JC Murray, HF Willard, KF Nolan, KB Reid, DJ Blake, S Lindsay, SS Bhattacharya, A Wright, KE Davies, Genetic and physical mapping around the properdin P gene., Genomics, UNITED STATES, vol. 11 no. 4 (December, 1991), pp. 991-6  [abs].
  119. HF Willard, Evolution of alpha satellite., Current opinion in genetics & development, ENGLAND, vol. 1 no. 4 (December, 1991), pp. 509-14  [abs].
  120. PE Warburton, GM Greig, T Haaf, HF Willard, PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis., Genomics, UNITED STATES, vol. 11 no. 2 (October, 1991), pp. 324-33  [abs].
  121. RG Lafrenière, CJ Brown, VE Powers, L Carrel, KE Davies, DF Barker, HF Willard, Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome., Genomics, UNITED STATES, vol. 11 no. 2 (October, 1991), pp. 352-63  [abs].
  122. AP Losada, M Wessman, M Tiainen, AH Hopman, HF Willard, F Solé, MR Caballín, S Woessner, S Knuutila, Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study., Blood, UNITED STATES, vol. 78 no. 3 (August, 1991), pp. 775-9  [abs].
  123. MM Mahtani, RG Lafrenière, TA Kruse, HF Willard, An 18-locus linkage map of the pericentromeric region of the human X chromosome: genetic framework for mapping X-linked disorders., Genomics, UNITED STATES, vol. 10 no. 4 (August, 1991), pp. 849-57  [abs].
  124. CU Kirchgessner, JA Trofatter, MM Mahtani, HF Willard, LJ DeGennaro, A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes., American journal of human genetics, UNITED STATES, vol. 49 no. 1 (July, 1991), pp. 184-91  [abs].
  125. J Fujii, A Zarain-Herzberg, HF Willard, M Tada, DH MacLennan, Structure of the rabbit phospholamban gene, cloning of the human cDNA, and assignment of the gene to human chromosome 6., The Journal of biological chemistry, UNITED STATES, vol. 266 no. 18 (June, 1991), pp. 11669-75  [abs].
  126. RG Lafreniere, MT Geraghty, D Valle, TB Shows, HF Willard, Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm., Genomics, UNITED STATES, vol. 10 no. 1 (May, 1991), pp. 276-9  [abs].
  127. R Wevrick, HF Willard, Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays., Nucleic acids research, ENGLAND, vol. 19 no. 9 (May, 1991), pp. 2295-301  [abs].
  128. M Trifiro, B Gottlieb, L Pinsky, M Kaufman, L Prior, DD Belsham, K Wrogemann, CJ Brown, HF Willard, J Trapman, The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene., Molecular and cellular endocrinology, NETHERLANDS, vol. 75 no. 1 (January, 1991), pp. 37-47  [abs].
  129. CJ Brown, RG Lafreniere, VE Powers, G Sebastio, A Ballabio, AL Pettigrew, DH Ledbetter, E Levy, IW Craig, HF Willard, Localization of the X inactivation centre on the human X chromosome in Xq13., Nature, ENGLAND, vol. 349 no. 6304 (January, 1991), pp. 82-4  [abs].
  130. CJ Brown, A Ballabio, JL Rupert, RG Lafreniere, M Grompe, R Tonlorenzi, HF Willard, A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome., Nature, ENGLAND, vol. 349 no. 6304 (January, 1991), pp. 38-44  [abs].
  131. GM Greig, S Parikh, J George, VE Powers, HF Willard, Molecular cytogenetics of alpha satellite DNA from chromosome 12: fluorescence in situ hybridization and description of DNA and array length polymorphisms., Cytogenetics and cell genetics, SWITZERLAND, vol. 56 no. 3-4 (1991), pp. 144-8  [abs].
  132. RG Taylor, J García-Heras, SJ Sadler, RG Lafreniere, HF Willard, DH Ledbetter, RR McInnes, Localization of histidase to human chromosome region 12q22----q24.1 and mouse chromosome region 10C2----D1., Cytogenetics and cell genetics, SWITZERLAND, vol. 56 no. 3-4 (1991), pp. 178-81  [abs].
  133. KG Ten Hagen, DM Gilbert, HF Willard, SN Cohen, Replication timing of DNA sequences associated with human centromeres and telomeres., Molecular and cellular biology, UNITED STATES, vol. 10 no. 12 (December, 1990), pp. 6348-55  [abs].
  134. HF Willard, Centromeres of mammalian chromosomes., Trends in genetics : TIG, ENGLAND, vol. 6 no. 12 (December, 1990), pp. 410-6  [abs].
  135. R Wevrick, WC Earnshaw, PN Howard-Peebles, HF Willard, Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangement., Molecular and cellular biology, UNITED STATES, vol. 10 no. 12 (December, 1990), pp. 6374-80  [abs].
  136. EM Fisher, P Beer-Romero, LG Brown, A Ridley, JA McNeil, JB Lawrence, HF Willard, FR Bieber, DC Page, Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome., Cell, UNITED STATES, vol. 63 no. 6 (December, 1990), pp. 1205-18  [abs].
  137. K Chun, N Mackay, HF Willard, BH Robinson, Isolation, characterization and chromosomal localization of cDNA clones for the E1 beta subunit of the pyruvate dehydrogenase complex., European journal of biochemistry / FEBS, GERMANY, vol. 194 no. 2 (December, 1990), pp. 587-92  [abs].
  138. SJ Durfy, HF Willard, Concerted evolution of primate alpha satellite DNA. Evidence for an ancestral sequence shared by gorilla and human X chromosome alpha satellite., Journal of molecular biology, ENGLAND, vol. 216 no. 3 (December, 1990), pp. 555-66  [abs].
  139. PE Warburton, HF Willard, Genomic analysis of sequence variation in tandemly repeated DNA. Evidence for localized homogeneous sequence domains within arrays of alpha-satellite DNA., Journal of molecular biology, ENGLAND, vol. 216 no. 1 (November, 1990), pp. 3-16  [abs].
  140. VM Watt, HF Willard, The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysis., Human genetics, GERMANY, vol. 85 no. 6 (October, 1990), pp. 651-4  [abs].
  141. RA Norum, RG Lafreniere, LW O'Neal, TF Nikolai, JP Delaney, JC Sisson, H Sobol, GM Lenoir, BA Ponder, HF Willard, Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A., Genomics, UNITED STATES, vol. 8 no. 2 (October, 1990), pp. 313-7  [abs].
  142. T Ozçelik, RG Lafreniere, BT Archer, PA Johnston, HF Willard, U Francke, TC Südhof, Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse., American journal of human genetics, UNITED STATES, vol. 47 no. 3 (September, 1990), pp. 551-61  [abs].
  143. MM Mahtani, HF Willard, Pulsed-field gel analysis of alpha-satellite DNA at the human X chromosome centromere: high-frequency polymorphisms and array size estimate., Genomics, UNITED STATES, vol. 7 no. 4 (August, 1990), pp. 607-13  [abs].
  144. CB Sharp, HM Bedford, HF Willard, Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity., Human genetics, GERMANY, WEST, vol. 85 no. 3 (August, 1990), pp. 330-6  [abs].
  145. K Otsu, HF Willard, VK Khanna, F Zorzato, NM Green, DH MacLennan, Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum., The Journal of biological chemistry, UNITED STATES, vol. 265 no. 23 (August, 1990), pp. 13472-83  [abs].
  146. CJ Brown, AM Flenniken, BR Williams, HF Willard, X chromosome inactivation of the human TIMP gene., Nucleic acids research, ENGLAND, vol. 18 no. 14 (July, 1990), pp. 4191-5  [abs].
  147. RG Lafreniere, HF Willard, A BstE II RFLP at the DXS153 locus., Nucleic acids research, ENGLAND, vol. 18 no. 12 (June, 1990), pp. 3673 .
  148. RG Lafreniere, HF Willard, A Rsal RFLP at the DXS467 locus., Nucleic acids research, ENGLAND, vol. 18 no. 12 (June, 1990), pp. 3673 .
  149. AE MacKenzie, RG Korneluk, F Zorzato, J Fujii, M Phillips, D Iles, B Wieringa, S Leblond, J Bailly, HF Willard, The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy., American journal of human genetics, UNITED STATES, vol. 46 no. 6 (June, 1990), pp. 1082-9  [abs].
  150. JT Clarke, HF Willard, I Teshima, PL Chang, MA Skomorowski, Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girl., Clinical genetics, DENMARK, vol. 37 no. 5 (May, 1990), pp. 355-62  [abs].
  151. JA Luty, Z Guo, HF Willard, DH Ledbetter, S Ledbetter, M Litt, Five polymorphic microsatellite VNTRs on the human X chromosome., American journal of human genetics, UNITED STATES, vol. 46 no. 4 (April, 1990), pp. 776-83  [abs].
  152. J Fujii, HF Willard, DH MacLennan, Characterization and localization to human chromosome 1 of human fast-twitch skeletal muscle calsequestrin gene., Somatic cell and molecular genetics, UNITED STATES, vol. 16 no. 2 (March, 1990), pp. 185-9  [abs].
  153. J Koch, S Kølvraa, N Hobolt, GB Petersen, HF Willard, JS Waye, N Gregersen, L Bolund, A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization., Clinical genetics, DENMARK, vol. 37 no. 3 (March, 1990), pp. 216-20  [abs].
  154. CJ Brown, HF Willard, Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation., American journal of human genetics, UNITED STATES, vol. 46 no. 2 (February, 1990), pp. 273-9  [abs].
  155. KE Davies, JL Mandel, AP Monaco, RL Nussbaum, HF Willard, Report of the committee on the genetic constitution of the X chromosome., Cytogenetics and cell genetics, SWITZERLAND, vol. 55 no. 1-4 (1990), pp. 254-313 .
  156. HF Willard, Alpha and beta satellite sequences on chromosome 21: the possible role of centromere and chromosome structure in nondisjunction., Progress in clinical and biological research, UNITED STATES, vol. 360 (1990), pp. 39-52 .
  157. P Shier, HF Willard, VM Watt, Localization of the insulin receptor-related receptor gene to human chromosome 1., Cytogenetics and cell genetics, SWITZERLAND, vol. 54 no. 1-2 (1990), pp. 80-1  [abs].
  158. JN Dietz-Band, AE Turco, HF Willard, A Vincent, MH Skolnick, DF Barker, Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers., Cytogenetics and cell genetics, SWITZERLAND, vol. 54 no. 3-4 (1990), pp. 137-41  [abs].
  159. R Wevrick, HF Willard, Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 86 no. 23 (December, 1989), pp. 9394-8  [abs].
  160. GM Greig, SB England, HM Bedford, HF Willard, Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16., American journal of human genetics, UNITED STATES, vol. 45 no. 6 (December, 1989), pp. 862-72  [abs].
  161. SJ Durfy, HF Willard, Patterns of intra- and interarray sequence variation in alpha satellite from the human X chromosome: evidence for short-range homogenization of tandemly repeated DNA sequences., Genomics, UNITED STATES, vol. 5 no. 4 (November, 1989), pp. 810-21  [abs].
  162. WL Greer, MM Mahtani, PC Kwong, LA Rubin, M Peacocke, HF Willard, KA Siminovitch, Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction., Human genetics, GERMANY, WEST, vol. 83 no. 3 (October, 1989), pp. 227-30  [abs].
  163. R Tran-Paterson, HF Willard, M Letarte, The common acute lymphoblastic leukemia antigen (neutral endopeptidase-3.4.24.11) gene is located on human chromosome 3., Cancer genetics and cytogenetics, UNITED STATES, vol. 42 no. 1 (October, 1989), pp. 129-34  [abs].
  164. JS Waye, HF Willard, Concerted evolution of alpha satellite DNA: evidence for species specificity and a general lack of sequence conservation among alphoid sequences of higher primates., Chromosoma, GERMANY, WEST, vol. 98 no. 4 (October, 1989), pp. 273-9  [abs].
  165. CJ Brown, HF Willard, Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect., American journal of human genetics, UNITED STATES, vol. 45 no. 4 (October, 1989), pp. 592-8  [abs].
  166. RG Lafreniere, MM Mahtani, HF Willard, An X-linked DraI RFLP recognized by cpX23 [DXS132], Nucleic acids research, ENGLAND, vol. 17 no. 16 (August, 1989), pp. 6754 .
  167. JS Waye, HF Willard, Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 86 no. 16 (August, 1989), pp. 6250-4  [abs].
  168. JS Waye, HF Willard, Chromosome specificity of satellite DNAs: short- and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3., Chromosoma, GERMANY, WEST, vol. 97 no. 6 (May, 1989), pp. 475-80  [abs].
  169. CJ Brown, VE Powers, DL Munroe, R Sheinin, HF Willard, Gene on short arm of human X chromosome complements murine tsA1S9 DNA synthesis mutation., Somatic cell and molecular genetics, UNITED STATES, vol. 15 no. 2 (March, 1989), pp. 173-8  [abs].
  170. HF Willard, SJ Durfy, MM Mahtani, H Dorkins, KE Davies, BR Williams, Regional localization of the TIMP gene on the human X chromosome. Extension of a conserved synteny and linkage group on proximal Xp., Human genetics, GERMANY, WEST, vol. 81 no. 3 (February, 1989), pp. 234-8  [abs].
  171. C Logan, HF Willard, JM Rommens, AL Joyner, Chromosomal localization of the human homeo box-containing genes, EN1 and EN2., Genomics, UNITED STATES, vol. 4 no. 2 (February, 1989), pp. 206-9  [abs].
  172. CJ Brown, SJ Goss, DB Lubahn, DR Joseph, EM Wilson, FS French, HF Willard, Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism., American journal of human genetics, UNITED STATES, vol. 44 no. 2 (February, 1989), pp. 264-9  [abs].
  173. CJ Brown, T Sekiguchi, T Nishimoto, HF Willard, Regional localization of CCG1 gene which complements hamster cell cycle mutation BN462 to Xq11-Xq13., Somatic cell and molecular genetics, UNITED STATES, vol. 15 no. 1 (January, 1989), pp. 93-6  [abs].
  174. PR Fain, E Wright, HF Willard, K Stephens, DF Barker, The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints., American journal of human genetics, UNITED STATES, vol. 44 no. 1 (January, 1989), pp. 68-72  [abs].
  175. K Stephens, P Green, VM Riccardi, S Ng, M Rising, D Barker, JK Darby, KM Falls, FS Collins, HF Willard, Genetic analysis of eight loci tightly linked to neurofibromatosis 1., American journal of human genetics, UNITED STATES, vol. 44 no. 1 (January, 1989), pp. 13-9  [abs].
  176. KK Kidd, AM Bowcock, J Schmidtke, RK Track, F Ricciuti, G Hutchings, A Bale, P Pearson, HF Willard, J Gelernter, Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms., Cytogenetics and cell genetics, SWITZERLAND, vol. 51 no. 1-4 (1989), pp. 622-947 .
  177. HF Willard, R Wevrick, PE Warburton, Human centromere structure: organization and potential role of alpha satellite DNA., Progress in clinical and biological research, UNITED STATES, vol. 318 (1989), pp. 9-18 .
  178. T Alitalo, HF Willard, A de la Chapelle, Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7., Cytogenetics and cell genetics, SWITZERLAND, vol. 50 no. 1 (1989), pp. 49-53  [abs].
  179. HF Willard, The genomics of long tandem arrays of satellite DNA in the human genome., Genome / National Research Council Canada = Génome / Conseil national de recherches Canada, CANADA, vol. 31 no. 2 (1989), pp. 737-44  [abs].
  180. JL Mandel, HF Willard, RL Nussbaum, G Romeo, JM Puck, KE Davies, Report of the committee on the genetic constitution of the X chromosome., Cytogenetics and cell genetics, SWITZERLAND, vol. 51 no. 1-4 (1989), pp. 384-437 .
  181. CJ Brown, MM Mahtani, HF Willard, Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome., Human genetics, GERMANY, WEST, vol. 80 no. 3 (November, 1988), pp. 296-8  [abs].
  182. P Devilee, RF Thierry, T Kievits, R Kolluri, AH Hopman, HF Willard, PL Pearson, CJ Cornelisse, Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes., Cancer research, UNITED STATES, vol. 48 no. 20 (October, 1988), pp. 5825-30  [abs].
  183. GA Mitchell, JE Looney, LC Brody, G Steel, M Suchanek, JF Engelhardt, HF Willard, D Valle, Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene., The Journal of biological chemistry, UNITED STATES, vol. 263 no. 28 (October, 1988), pp. 14288-95  [abs].
  184. G Otulakowski, BH Robinson, HF Willard, Gene for lipoamide dehydrogenase maps to human chromosome 7., Somatic cell and molecular genetics, UNITED STATES, vol. 14 no. 4 (July, 1988), pp. 411-4  [abs].
  185. P Devilee, T Kievits, JS Waye, PL Pearson, HF Willard, Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10., Genomics, UNITED STATES, vol. 3 no. 1 (July, 1988), pp. 1-7  [abs].
  186. MM Mahtani, HF Willard, A primary genetic map of the pericentromeric region of the human X chromosome., Genomics, UNITED STATES, vol. 2 no. 4 (May, 1988), pp. 294-301  [abs].
  187. DB Lubahn, DR Joseph, PM Sullivan, HF Willard, FS French, EM Wilson, Cloning of human androgen receptor complementary DNA and localization to the X chromosome., Science (New York, N.Y.), UNITED STATES, vol. 240 no. 4850 (April, 1988), pp. 327-30  [abs].
  188. R Allore, D O'Hanlon, R Price, K Neilson, HF Willard, DR Cox, A Marks, RJ Dunn, Gene encoding the beta subunit of S100 protein is on chromosome 21: implications for Down syndrome., Science (New York, N.Y.), UNITED STATES, vol. 239 no. 4845 (March, 1988), pp. 1311-3  [abs].
  189. JS Waye, RA Gravel, HF Willard, Two PstI RFLPs in the PCCB gene on the long arm of chromosome 3., Nucleic acids research, ENGLAND, vol. 16 no. 5 (March, 1988), pp. 2362 .
  190. JE Spence, RG Perciaccante, GM Greig, HF Willard, DH Ledbetter, JF Hejtmancik, MS Pollack, WE O'Brien, AL Beaudet, Uniparental disomy as a mechanism for human genetic disease., American journal of human genetics, UNITED STATES, vol. 42 no. 2 (February, 1988), pp. 217-26  [abs].
  191. JS Waye, AR Mitchell, HF Willard, Organization and genomic distribution of "82H" alpha satellite DNA. Evidence for a low-copy or single-copy alphoid domain located on human chromosome 14., Human genetics, GERMANY, WEST, vol. 78 no. 1 (January, 1988), pp. 27-32  [abs].
  192. RG Worton, J Sutherland, JE Sylvester, HF Willard, S Bodrug, I Dubé, C Duff, V Kean, PN Ray, RD Schmickel, Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end., Science (New York, N.Y.), UNITED STATES, vol. 239 no. 4835 (January, 1988), pp. 64-8  [abs].
  193. JL Mandel, HF Willard, RL Nussbaum, KE Davies, G Romeo, Report of the committee on the genetic constitution of the X chromosome., Cytogenetics and cell genetics, SWITZERLAND, vol. 49 no. 1-3 (1988), pp. 107-28 .
  194. KK Kidd, AM Bowcock, PL Pearson, J Schmidtke, HF Willard, RK Track, F Ricciuti, Report of the committee on human gene mapping by recombinant DNA techniques., Cytogenetics and cell genetics, SWITZERLAND, vol. 49 no. 1-3 (1988), pp. 132-218 .
  195. P Tsipouras, RC Schwartz, JA Phillips, HF Willard, A centromere-based linkage group on the long arm of human chromosome 17., Cytogenetics and cell genetics, SWITZERLAND, vol. 47 no. 1-2 (1988), pp. 109-10  [abs].
  196. HF Willard, GM Greig, VE Powers, JS Waye, Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: implications for linkage in neurofibromatosis., Genomics, UNITED STATES, vol. 1 no. 4 (December, 1987), pp. 368-73  [abs].
  197. CJ Brown, HF Willard, MspI RFLP detected with chromosome-walk clone pXUT23-SE3.2L from DXS16 in Xp22.1-22.3., Nucleic acids research, ENGLAND, vol. 15 no. 22 (November, 1987), pp. 9614 .
  198. JS Waye, GM Greig, HF Willard, Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11., Human genetics, GERMANY, WEST, vol. 77 no. 2 (October, 1987), pp. 151-6  [abs].
  199. SJ Durfy, HF Willard, Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosome., American journal of human genetics, UNITED STATES, vol. 41 no. 3 (September, 1987), pp. 391-401  [abs].
  200. JS Waye, HF Willard, Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes., Nucleic acids research, ENGLAND, vol. 15 no. 18 (September, 1987), pp. 7549-69  [abs].
  201. JS Waye, SJ Durfy, D Pinkel, S Kenwrick, M Patterson, KE Davies, HF Willard, Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA., Genomics, UNITED STATES, vol. 1 no. 1 (September, 1987), pp. 43-51  [abs].
  202. B Vogelstein, ER Fearon, SR Hamilton, AC Preisinger, HF Willard, AM Michelson, AD Riggs, SH Orkin, Clonal analysis using recombinant DNA probes from the X-chromosome., Cancer research, UNITED STATES, vol. 47 no. 18 (September, 1987), pp. 4806-13  [abs].
  203. L Mengle-Gaw, HF Willard, CI Smith, L Hammarström, P Fischer, P Sherrington, G Lucas, PW Thompson, R Baer, TH Rabbitts, Human T-cell tumours containing chromosome 14 inversion or translocation with breakpoints proximal to immunoglobulin joining regions at 14q32., The EMBO journal, ENGLAND, vol. 6 no. 8 (August, 1987), pp. 2273-80  [abs].
  204. DH MacLennan, CJ Brandl, S Champaneria, PC Holland, VE Powers, HF Willard, Fast-twitch and slow-twitch/cardiac Ca2+ ATPase genes map to human chromosomes 16 and 12., Somatic cell and molecular genetics, UNITED STATES, vol. 13 no. 4 (July, 1987), pp. 341-6  [abs].
  205. BF O'Dowd, K Neote, DL Munroe, RA Gravel, D Mahuran, HF Willard, PstI RFLP in the human hexosaminidase (HEXB) gene on chromosome 5., Nucleic acids research, ENGLAND, vol. 15 no. 7 (April, 1987), pp. 3194 .
  206. DR Bell, JM Trent, HF Willard, JR Riordan, V Ling, Chromosomal location of human P-glycoprotein gene sequences., Cancer genetics and cytogenetics, UNITED STATES, vol. 25 no. 1 (March, 1987), pp. 141-8  [abs].
  207. JS Wu, JR Riordan, HF Willard, R Milner, KK Kidd, MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA clone., Nucleic acids research, ENGLAND, vol. 15 no. 4 (February, 1987), pp. 1882 .
  208. JS Waye, SB England, HF Willard, Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome., Molecular and cellular biology, UNITED STATES, vol. 7 no. 1 (January, 1987), pp. 349-56  [abs].
  209. HF Willard, JS Waye, Chromosome-specific subsets of human alpha satellite DNA: analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat., Journal of molecular evolution, UNITED STATES, vol. 25 no. 3 (1987), pp. 207-14  [abs].
  210. PL Pearson, KK Kidd, HF Willard, Report of the committee on human gene mapping by recombinant DNA techniques., Cytogenetics and cell genetics, SWITZERLAND, vol. 46 no. 1-4 (1987), pp. 390-566 .
  211. JS Waye, LA Creeper, HF Willard, Organization and evolution of alpha satellite DNA from human chromosome 11., Chromosoma, GERMANY, WEST, vol. 95 no. 3 (1987), pp. 182-8  [abs].
  212. SJ Durfy, SC Clark, BR Williams, HF Willard, RFLP detected by an X-linked cDNA encoding erythroid-potentiating activity/tissue inhibitor of metalloproteinase (EPA/TIMP)., Nucleic acids research, ENGLAND, vol. 14 no. 22 (November, 1986), pp. 9226 .
  213. BF O'Dowd, MH Klavins, HF Willard, R Gravel, JA Lowden, DJ Mahuran, Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis)., The Journal of biological chemistry, UNITED STATES, vol. 261 no. 27 (September, 1986), pp. 12680-5  [abs].
  214. JS Waye, HF Willard, Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixation., Nucleic acids research, ENGLAND, vol. 14 no. 17 (September, 1986), pp. 6915-27  [abs].
  215. JS Waye, HF Willard, Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome., Molecular and cellular biology, UNITED STATES, vol. 6 no. 9 (September, 1986), pp. 3156-65  [abs].
  216. J Squire, TP Dryja, J Dunn, A Goddard, T Hofmann, M Musarella, HF Willard, AJ Becker, BL Gallie, RA Phillips, Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 83 no. 17 (September, 1986), pp. 6573-7  [abs].
  217. HF Willard, JS Waye, MH Skolnick, CE Schwartz, VE Powers, SB England, Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 83 no. 15 (August, 1986), pp. 5611-5  [abs].
  218. NE Cooke, HF Willard, EV David, DL George, Direct regional assignment of the gene for vitamin D binding protein (Gc-globulin) to human chromosome 4q11-q13 and identification of an associated DNA polymorphism., Human genetics, GERMANY, WEST, vol. 73 no. 3 (July, 1986), pp. 225-9  [abs].
  219. AM Lamhonwah, TJ Barankiewicz, HF Willard, DJ Mahuran, F Quan, RA Gravel, Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 83 no. 13 (July, 1986), pp. 4864-8  [abs].
  220. BR Williams, ME Saunders, HF Willard, Interferon-regulated human 2-5A synthetase gene maps to chromosome 12., Somatic cell and molecular genetics, UNITED STATES, vol. 12 no. 4 (July, 1986), pp. 403-8  [abs].
  221. RG Korneluk, DJ Mahuran, K Neote, MH Klavins, BF O'Dowd, M Tropak, HF Willard, MJ Anderson, JA Lowden, RA Gravel, Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease., The Journal of biological chemistry, UNITED STATES, vol. 261 no. 18 (June, 1986), pp. 8407-13  [abs].
  222. LC Tsui, S Zengerling, HF Willard, M Buchwald, Mapping of the cystic fibrosis locus on chromosome 7., Cold Spring Harbor symposia on quantitative biology, UNITED STATES, vol. 51 Pt 1 (1986), pp. 325-35 .
  223. M Buchwald, M Zsiga, D Markiewicz, N Plavsic, D Kennedy, S Zengerling, HF Willard, P Tsipouras, K Schmiegelow, M Schwartz, Linkage of cystic fibrosis to the pro alpha 2(I) collagen gene, COL1A2, on chromosome 7., Cytogenetics and cell genetics, SWITZERLAND, vol. 41 no. 4 (1986), pp. 234-9  [abs].
  224. HF Willard, JR Riordan, Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders., Science (New York, N.Y.), UNITED STATES, vol. 230 no. 4728 (November, 1985), pp. 940-2  [abs].
  225. HF Willard, SO Meakin, LC Tsui, ML Breitman, Assignment of human gamma crystallin multigene family to chromosome 2., Somatic cell and molecular genetics, UNITED STATES, vol. 11 no. 5 (September, 1985), pp. 511-6  [abs].
  226. BJ Schmeckpeper, J Davis, HF Willard, KD Smith, An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22 [HGM8 provisional no. DXS72]., Nucleic acids research, ENGLAND, vol. 13 no. 15 (August, 1985), pp. 5724 .
  227. HF Willard, Chromosome-specific organization of human alpha satellite DNA., American journal of human genetics, UNITED STATES, vol. 37 no. 3 (May, 1985), pp. 524-32  [abs].
  228. C Ingle, R Williamson, A de la Chapelle, RR Herva, K Haapala, G Bates, HF Willard, P Pearson, KE Davies, Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation., American journal of human genetics, UNITED STATES, vol. 37 no. 3 (May, 1985), pp. 451-62  [abs].
  229. J Wolfe, SM Darling, RP Erickson, IW Craig, VJ Buckle, PW Rigby, HF Willard, PN Goodfellow, Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome., Journal of molecular biology, ENGLAND, vol. 182 no. 4 (April, 1985), pp. 477-85  [abs].
  230. JS Waye, HF Willard, Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome., Nucleic acids research, ENGLAND, vol. 13 no. 8 (April, 1985), pp. 2731-43  [abs].
  231. E Bakker, MH Hofker, N Goor, JL Mandel, K Wrogemann, KE Davies, LM Kunkel, HF Willard, WA Fenton, L Sandkuyl, Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs., Lancet, ENGLAND, vol. 1 no. 8430 (March, 1985), pp. 655-8  [abs].
  232. JS Rubin, VR Prideaux, HF Willard, AM Dulhanty, GF Whitmore, A Bernstein, Molecular cloning and chromosomal localization of DNA sequences associated with a human DNA repair gene., Molecular and cellular biology, UNITED STATES, vol. 5 no. 2 (February, 1985), pp. 398-405  [abs].
  233. BF O'Dowd, F Quan, HF Willard, AM Lamhonwah, RG Korneluk, JA Lowden, RA Gravel, DJ Mahuran, Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 82 no. 4 (February, 1985), pp. 1184-8  [abs].
  234. EE Michalopoulos, PJ Bevilacqua, N Stokoe, VE Powers, HF Willard, WH Lewis, Molecular analysis of gene deletion in aniridia--Wilms tumor association., Human genetics, GERMANY, WEST, vol. 70 no. 2 (1985), pp. 157-62  [abs].
  235. WH Lewis, JM Goguen, VE Powers, HF Willard, EE Michalopoulos, Gene order on the short arm of human chromosome 11: regional assignment of the LDH A gene distal to catalase in two translocations., Human genetics, GERMANY, WEST, vol. 71 no. 3 (1985), pp. 249-53  [abs].
  236. HF Willard, SJ Goss, MT Holmes, DL Munroe, Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19., Human genetics, GERMANY, WEST, vol. 71 no. 2 (1985), pp. 138-43  [abs].
  237. HF Willard, MH Skolnick, PL Pearson, JL Mandel, Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques., Cytogenetics and cell genetics, SWITZERLAND, vol. 40 no. 1-4 (1985), pp. 360-489 .
  238. RG Korneluk, F Quan, WH Lewis, KS Guise, HF Willard, MT Holmes, RA Gravel, Isolation of human fibroblast catalase cDNA clones. Sequence of clones derived from spliced and unspliced mRNA., The Journal of biological chemistry, UNITED STATES, vol. 259 no. 22 (November, 1984), pp. 13819-23  [abs].
  239. RG Worton, C Duff, JE Sylvester, RD Schmickel, HF Willard, Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes., Science (New York, N.Y.), UNITED STATES, vol. 224 no. 4656 (June, 1984), pp. 1447-9  [abs].
  240. MH Skolnick, HF Willard, LA Menlove, Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques., Cytogenetics and cell genetics, SWITZERLAND, vol. 37 no. 1-4 (1984), pp. 210-73 .
  241. HF Willard, MT Holmes, A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids., Human genetics, GERMANY, WEST, vol. 66 no. 2-3 (1984), pp. 272-5  [abs].
  242. HF Willard, KD Smith, J Sutherland, Isolation and characterization of a major tandem repeat family from the human X chromosome., Nucleic acids research, ENGLAND, vol. 11 no. 7 (April, 1983), pp. 2017-33  [abs].
  243. WA Fenton, AM Hack, HF Willard, A Gertler, LE Rosenberg, Purification and properties of methylmalonyl coenzyme A mutase from human liver., Archives of biochemistry and biophysics, UNITED STATES, vol. 214 no. 2 (April, 1982), pp. 815-23 .
  244. BJ Schmeckpeper, HF Willard, KD Smith, Isolation and characterization of cloned human DNA fragments carrying reiterated sequences common to both autosomes and the X chromosome., Nucleic acids research, ENGLAND, vol. 9 no. 8 (April, 1981), pp. 1853-72  [abs].
  245. HF Willard, WR Breg, Human X chromosomes: synchrony of DNA replication in diploid and triploid fibroblasts with multiple active or inactive X chromosomes., Somatic cell genetics, UNITED STATES, vol. 6 no. 2 (March, 1980), pp. 187-98  [abs].
  246. HF Willard, LE Rosenberg, Interactions of methylmalonyl CoA mutase from normal human fibroblasts with adenosylcobalamin and methylmalonyl CoA: evidence for non-equivalent active sites., Archives of biochemistry and biophysics, UNITED STATES, vol. 200 no. 1 (March, 1980), pp. 130-9 .
  247. HF Willard, LE Rosenberg, Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression., The Journal of clinical investigation, UNITED STATES, vol. 65 no. 3 (March, 1980), pp. 690-8  [abs].
  248. B Wolf, HF Willard, LE Rosenberg, Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts., American journal of human genetics, UNITED STATES, vol. 32 no. 1 (January, 1980), pp. 16-25  [abs].
  249. I Mellman, HF Willard, P Youngdahl-Turner, LE Rosenberg, Cobalamin coenzyme synthesis in normal and mutant human fibroblasts. Evidence for a processing enzyme activity deficient in cblC cells., The Journal of biological chemistry, UNITED STATES, vol. 254 no. 23 (December, 1979), pp. 11847-53 .
  250. HF Willard, LE Rosenberg, Inborn errors of cobalamin metabolism: effect of cobalamin supplementation in culture on methylmalonyl CoA mutase activity in normal and mutant human fibroblasts., Biochemical genetics, UNITED STATES, vol. 17 no. 1-2 (February, 1979), pp. 57-75  [abs].
  251. I Mellman, HF Willard, LE Rosenberg, Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts., The Journal of clinical investigation, UNITED STATES, vol. 62 no. 5 (November, 1978), pp. 952-60  [abs].
  252. HF Willard, IS Mellman, LE Rosenberg, Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant., American journal of human genetics, UNITED STATES, vol. 30 no. 1 (January, 1978), pp. 1-13 .
  253. HF Willard, LE Rosenberg, Inherited deficiencies of human methylmalonyl CaA mutase activity: reduced affinity of mutant apoenzyme for adenosylcobalamin., Biochemical and biophysical research communications, UNITED STATES, vol. 78 no. 3 (October, 1977), pp. 927-34 .
  254. HF Willard, Tissue-specific heterogeneity in DNA replication patterns of human X chromosomes., Chromosoma, GERMANY, WEST, vol. 61 no. 1 (April, 1977), pp. 61-73 .
  255. IS Mellman, P Youngdahl-Turner, HF Willard, LE Rosenberg, Intracellular binding of radioactive hydroxocobalamin to cobalamin-dependent apoenzymes in rat liver., Proceedings of the National Academy of Sciences of the United States of America, UNITED STATES, vol. 74 no. 3 (March, 1977), pp. 916-20  [abs].
  256. HF Willard, LM Ambani, AC Hart, MJ Mahoney, LE Rosenberg, Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells., Human genetics, GERMANY, WEST, vol. 34 no. 3 (December, 1976), pp. 277-83  [abs].
  257. SA Latt, HF Willard, PS Gerald, BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes., Chromosoma, GERMANY, WEST, vol. 57 no. 2 (August, 1976), pp. 135-53  [abs].
  258. HF Willard, SA Latt, Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy., American journal of human genetics, UNITED STATES, vol. 28 no. 3 (May, 1976), pp. 213-27  [abs].
  259. SA Latt, G Stetten, LA Juergens, HF Willard, CD Scher, Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence., The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, UNITED STATES, vol. 23 no. 7 (July, 1975), pp. 493-505  [abs].
  260. JM Friedman, M Blitzer, LJ Elsas, U Francke, HF Willard, Clinical objectives in medical genetics for undergraduate medical students. Association of Professors of Human Genetics, Clinical Objectives Task Force., Genetics in medicine : official journal of the American College of Medical Genetics, United States, vol. 1 no. 1 , pp. 54-5 .
  261. T Glaser, WH Lewis, GA Bruns, PC Watkins, CE Rogler, TB Shows, VE Powers, HF Willard, JM Goguen, KO Simola, The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus., Nature, ENGLAND, vol. 321 no. 6073 , pp. 882-7  [abs].

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