advertisement

---

Cortés-González V 1

Showing records 1 to 1 | Display all abstracts from Cortés-González V

69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Micheal S; Siddiqui SN; Zafar SN; Villanueva-Mendoza C; Cortés-González V; Khan MI; den Hollander AI
PLoS ONE 2016; 11: e0160016

---