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Rapp P 1
Showing records 1 to 1 | Display all abstracts from Rapp P17117 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
