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Results:
1-10
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Results: 10
Authors:
Ikeda, Yoshio
Dalton, Joline C.
Moseley, Melinda L.
Gardner, Kathy L.
Bird, Thomas D.
Ashizawa, Tetsuo
Seltzer, William K.
Pandolfo, Massimo
Milunsky, Aubrey
Potter, Nicholas T.
Shoji, Mikio
Vincent, John B.
Day, John W.
Ranum, Laura P.W.
Citation: Ikeda, Yoshio et al., Spinocerebellar Ataxia Type 8: Molecular Genetic Comparisonsand Haplotype Analysis of 37 Families with Ataxia, American journal of human genetics , 75(1), 2004, pp. 3-16
Authors:
Lebo, Roger V.
Lynch, Eric D.
Bird, Thomas D.
Golbus, Mitchell S.
Barker, David F.
O'Connell, Peter
Chance, Phillip F.
Citation: V. Lebo, Roger et al., Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers., American journal of human genetics , 50-I(1), 1992, pp. 42-55
Authors:
Raskind, Wendy H.
Wijsman, Ellen
Pagon, Roberta A.
Cox, Timothy C.
Bawden, Michael J.
May, Brian K.
Bird, Thomas D.
Citation: H. Raskind, Wendy et al., X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13., American journal of human genetics , 48-I(2), 1991, pp. 335-341
Authors:
Wijsman, Ellen M.
Warwick Daw, E.
Yu, Change-En
Payami, Haydeh
Steinbart, Ellen J.
Nochlin, David
Conlon, Erin M.
Bird, Thomas D.
Schellenberg, Gerard D.
Citation: M. Wijsman, Ellen et al., Evidence for a Novel Late-Onset Alzheimer Disease Locus on Chromosome 19p13.2, American journal of human genetics , 75(3), 2004, pp. 398-409
Authors:
Schellenberg, Gerard D.
Anderson, Leojean
O'dahl, Sheldon
Wisjman, Ellen M.
Sadovnick, Adele D.
Ball, Melvyn J.
Larson, Eric B.
Kukull, Walter A.
Martin, George M.
Roses, Allen D.
Bird, Thomas D.
Citation: D. Schellenberg, Gerard et al., APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease, American journal of human genetics , 49-I(3), 1991, pp. 511-517
Authors:
Schellenberg, Gerard D.
Pericak-Vance, Margaret A.
Wijsman, Ellen M.
Moore, Deborah K.
Gaskell, Perry C.
Yamaoka, Larry A.
Bebout, Jacqueline L.
Anderson, Leojean
Welsh, Kathleen A.
Clark, Christopher M.
Martin, George M.
Roses, Allen D.
Bird, Thomas D.
Citation: D. Schellenberg, Gerard et al., Linkage analysis of familial Alzheimer disease, using chromosome 21 markers, American journal of human genetics , 48-I(3), 1991, pp. 563-583
Authors:
Inoue, Ken
Osaka, Hitoshi
Thurston, Virginia C.
Clarke, Joe T.R.
Yoneyama, Akira
Rosenbarker, Lisa
Bird, Thomas D.
Hodes, M.E.
Shaffer, Lisa G.
Lupski, James R.
Citation: Inoue, Ken et al., Genomic Rearrangements Resulting in PLP1 Deletion Occur by Nonhomologous End Joining and Cause Different Dysmyelinating Phenotypes in Males and Females, American journal of human genetics , 71(4), 2002, pp. 838-853
Authors:
Chen, Dong-Hui
Brkanac, Zoran
Christophe Verlinde, L.M.J.
Tan, Xiao-Jian
Bylenok, Laura
Nochlin, David
Matsushita, Mark
Lipe, Hillary
Wolff, John
Fernandez, Magali
Cimino, P.J.
Bird, Thomas D.
Raskind, Wendy H.
Citation: Chen, Dong-hui et al., Missense Mutations in the Regulatory Domain of PKC.: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia, American journal of human genetics , 72(4), 2003, pp. 839-849
Authors:
Chance, Phillip F.
Bird, Thomas D.
O'Connell, Peter
Lipe, Hillary
Lalouel, Jean-Marc
Leppert, Mark
Citation: F. Chance, Phillip et al., Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I)., American journal of human genetics , 47-II(6), 1990, pp. 915-925
Authors:
Raskind, Wendy H.
Williams, Charles A.
Hudson, Lynn D.
Bird, Thomas D.
Citation: H. Raskind, Wendy et al., Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease., American journal of human genetics , 49-II(5), 1991, pp. 1355-1360
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