DOI: 10.1055/s-00029027

Journal of Pediatric Genetics

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

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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