M. Hamdani

Identification of 28 novel mutations in the Bardet–Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease

Jean Muller, Corinne Stoetzel, M. C. Vincent et al. · Human Genetics · 2010 · 132 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco

Ahmed Belmouden, Rahma Melki, M. Hamdani et al. · Clinical Genetics · 2002 · 70 citations

Life Sciences, Genetics, Molecular Genetics +17

[Cockayne's syndrome with unusual retinal involvement (report of one family)].

M. Hamdani, A. El Kettani, L. Raïs et al. · PubMed · 2000 · 10 citations

Medicine, Ophthalmology, Ocular Disease +9