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Brooks BP 1
Showing records 1 to 1 | Display all abstracts from Brooks BP10572 A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome
Brooks BP; Moroi SE; Downs CA; Wiltse S; Othman MI; Semina EV; Richards JE
Ophthalmic Genetics 2004; 25: 57-62
