DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Slavotinek AM, Chao R, Vacik T , et al.
VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans.
Hum Mutat 2012;
33 (2) 364-368
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