Authors:
Yu, Chang-En
Dawson, Geraldine
Munson, Jeffrey
D.Souza, Ian
Osterling, Julie
Estes, Annette
Leutenegger, Anne-Louise
Flodman, Pamela
Smith, Moyra
Raskind, Wendy H.
Spence, Anne M.
McMahon, William
Wijsman, Ellen M.
Schellenberg, Gerard D.
Citation: Yu, Chang-en et al., Presence of Large Deletions in Kindreds with Autism, American journal of human genetics , 71(1), 2002, pp. 100-115
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:
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:
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