Slavotinek et al., 2012
- VAX1 mutation associated with microphthalmia, corpus callosum agenesis and orofacial clefting-the first description of a VAX1 phenotype in humans.
Human Mutation
33(2):364-368
Full text @ Hum. Mutat.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | vax1 | ventral anterior homeobox 1 |
| Gene | vax2 | ventral anterior homeobox 2 |