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Tyler RC 1
Showing records 1 to 1 | Display all abstracts from Tyler RC54705 A Case of 22q11.2 Deletion Syndrome with Peters Anomaly, Congenital Glaucoma, and Heterozygous Mutation in CYP1B1
Reis LM; Tyler RC; Zori R; Burgess J; Mueller J; Semina EV
Ophthalmic Genetics 2015; 36: 92-94
