advertisement

---

Zeghidi H 2

Showing records 1 to 2 | Display all abstracts from Zeghidi H

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

---

17112 Ocular neovascularization in a patient with Fanconi anemia
Yahia SB; Touffahi SA; Zeghidi H; Zaouali S; Khairallah M
Canadian Journal of Ophthalmology 2006; 41: 778-779

---