![](/img/cover-not-exists.png)
Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies
Lucilene Arilho Ribeiro-Bicudo, Rodrigo G. Quiezi, Maria Leine Guion-Almeida, Chiara Legnaro, Antonio Richieri-CostaVolume:
158A
Year:
2012
Language:
english
Pages:
3
DOI:
10.1002/ajmg.a.35305
File:
PDF, 119 KB
english, 2012