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Camand O 1
Showing records 1 to 1 | Display all abstracts from Camand O17189 Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome
Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF
Molecular Vision 2006; 12: 1448-1460
