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Villanueva-Mendoza C 1

Showing records 1 to 1 | Display all abstracts from Villanueva-Mendoza C

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

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