Associated Papers
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate.
Nasser E et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2012
VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans.
Slavotinek AM et al.
Human Mutation, 2012
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