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Results:
1-10
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Results: 10
Authors:
Stephens, Karen
Green, Philip
Ricardi, Vincent M.
Ng, Siu
Rising, Marcia
Barker, David
Darby, John K.
Falls, Kathleen M.
Collins, Francis S.
Willard, Huntington F.
Donis-Keller, Helen
Citation: Stephens, Karen et al., Genetic analysis of eight loci tightly linked to neurofibromatosis I, American journal of human genetics , 44(1), 1989, pp. 13-19
Authors:
Kirchgessner, Cordula U.
Trofatter, James A.
Mahtani, Melanie M.
Willard, Huntington F.
DeGennaro, Louis J.
Citation: U. Kirchgessner, Cordula et al., 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 , 49-I(1), 1991, pp. 184-191
Authors:
Spence, Edward
Perciaccante, Ronald G.
Greig, Gillian M.
Willard, Huntington F.
Ledbetter, David H.
Heitmancik, J. Fielding
Pollack, Marilyn S.
O'Brien, William E.
Beaudet, Arthur L.
Citation: Spence, Edward et al., Uniparental disomy as a mechanism for human genetic disease, American journal of human genetics , 42(2), 1988, pp. 217-226
Authors:
Brown, Carolyn J.
Goss, Stephen J.
Lubahn, Dennis B.
Joseph, David R.
Wilson, Elizabeth M.
French, Frank S.
Willard, Huntington F.
Citation: J. Brown, Carolyn et al., Androgen receptor locus on the human x chromosome: regional localization to xg11-12 and description of a dna polymorphism, American journal of human genetics , 44(2), 1989, pp. 264-269
Authors:
Brown, Carolyn J.
Willard, Huntington F.
Citation: J. Brown, Carolyn et F. Willard, Huntington, Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation, American journal of human genetics , 46-I(2), 1990, pp. 273-279
Authors:
Durfy, Sharon J.
Willard, Huntington F.
Citation: J. Durfy, Sharon et F. Willard, Huntington, Molecular analysis of a polymorphic domain of apha satellite from the human X chromosome, American journal of human genetics , 41-I(3), 1987, pp. 391-401
Authors:
Ozçelik, Tayfun
Lafreniere, Ronald G.
Archer, Branch T.
Johnston, Patricia A.
Willard, Huntington F.
Francke, Uta
Südhof, Thomas C.
Citation: Ozçelik, Tayfun et al., Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse., American journal of human genetics , 47-I(3), 1990, pp. 551-561
Authors:
Brown, Carolyn J.
Willard, Huntington F.
Citation: J. Brown, Carolyn et F. Willard, Huntington, Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect, American journal of human genetics , 45-I(4), 1989, pp. 592-598
Authors:
Greig, Gillian M.
England, Sarah B.
Bedford, H. Melanie
Willard, Huntington F.
Citation: M. Greig, Gillian et al., Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16, American journal of human genetics , 45-II(6), 1989, pp. 862-872
Authors:
MacKenzie, Alex E.
Korneluk, Robert G.
Zorzato, Francesco
Fuji,Junichi
Phillips, Michael
lles, David
Wieringa, Bé
Leblond, Suzanne
Bailly, Jane
Willard, Huntington F.
Duff, Catherine
Worton, Ronald G.
MacLennan, David H.
Citation: E. Mackenzie, Alex et al., 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 , 46-II(6), 1990, pp. 1082-1089
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