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de la Houssaye G 2

Showing records 1 to 2 | Display all abstracts from de la Houssaye G

17117 Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report
de la Houssaye G; Bieche I; Roche O; Vieira V; Laurendeau I; Arbogast L; Zeghidi H; Rapp P; Halimi P; Vidaud M
BMC Medical Genetics 2006; 7: 82

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17189 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

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