S. Passemard
AuthID: R-00G-JTG
1
TITLE: WDR62 is associated with the spindle pole and is mutated in human microcephaly Full Text
AUTHORS: Nicholas, AK; Khurshid, M; Desir, J; Carvalho, OP; Cox, JJ; Thornton, G; Kausar, R; Ansar, M; Ahmad, W; Verloes, A; Passemard, S; Misson, JP; Lindsay, S; Gergely, F; Dobyns, WB; Roberts, E; Abramowicz, M; Woods, CG;
PUBLISHED: 2010, SOURCE: Nature Genetics, VOLUME: 42, ISSUE: 11
AUTHORS: Nicholas, AK; Khurshid, M; Desir, J; Carvalho, OP; Cox, JJ; Thornton, G; Kausar, R; Ansar, M; Ahmad, W; Verloes, A; Passemard, S; Misson, JP; Lindsay, S; Gergely, F; Dobyns, WB; Roberts, E; Abramowicz, M; Woods, CG;
PUBLISHED: 2010, SOURCE: Nature Genetics, VOLUME: 42, ISSUE: 11
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