AAAAAA

   
Results: 1-4 |
Results: 4

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
Risultati: 1-4 |