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Bosse KA 1
Showing records 1 to 1 | Display all abstracts from Bosse KA8814 Primary congenital glaucoma: a novel single-nucleotide deletion and varying phenotypic expression for the 1,546-1,555dup mutation in the GLC3A (CYP1B1) gene in 2 families of different ethnic origin
Soley GC; Bosse KA; Flikier D; Flikier P; Azofeifa J; Mardin CY; Reis A; Michels-Rautenstrauss KG; Rautenstrauss BW
Journal of Glaucoma 2003; 12: 27-30
