Bouchra Benazzouz

Gamma-D crystallin gene (<i>CRYGD</i>) mutation causes autosomal dominant congenital cerulean cataracts

Emeline F. Nandrot, C. Slingsby, A.K. Basak et al. · Journal of Medical Genetics · 2003 · 95 citations · Full text

Prevalence of metabolic syndrome and its components based on a harmonious definition among adults in Morocco

Omar Akhouayri, Otmane El Brini, Abdelhalem Mesfioui et al. · Diabetes Metabolic Syndrome and Obesity · 2014 · 48 citations · Full text

Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1.

Latifa Hilal, Soraya Boutayeb, Aziza Serrou et al. · PubMed · 2010 · 36 citations · Full text

Unusual Phenotypic Features in a Patient with a Novel Splice Mutation in the GHRHR Gene

Latifa Hilal, Yassir Hajaji, Marie-Pierre Vié-Luton et al. · Molecular Medicine · 2008 · 34 citations · Full text

Blood lead, cadmium and mercury among children from urban, industrial and rural areas of Fez Boulemane Region (Morocco): Relevant factors and early renal effects

Jawhar Laamech, Alfred Bernard, Xavier Dumont et al. · International Journal of Occupational Medicine and Environmental Health · 2014 · 27 citations · Full text