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VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: The first description of a VAX1 phenotype in humans

✍ Scribed by Anne M. Slavotinek; Ryan Chao; Tomas Vacik; Mani Yahyavi; Hana Abouzeid; Tanya Bardakjian; Adele Schneider; Gary Shaw; Elliott H. Sherr; Greg Lemke; Mohammed Youssef; Daniel F. Schorderet


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
182 KB
Volume
33
Category
Article
ISSN
1059-7794

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