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VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans
Authors:Slavotinek Anne M  Chao Ryan  Vacik Tomas  Yahyavi Mani  Abouzeid Hana  Bardakjian Tanya  Schneider Adele  Shaw Gary  Sherr Elliott H  Lemke Greg  Youssef Mohammed  Schorderet Daniel F
Affiliation:Department of Pediatrics, Division of Genetics, University of California, San Francisco, California 94143-0748, USA. slavotia@peds.ucsf.edu
Abstract:
Keywords:anophthalmia/microphthalmia  VAX1  VAX2  coloboma
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