F. El Kerch

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Fédérica Piccolo, Steven L. Roberds, Marc Jeanpierre et al. · Nature Genetics · 1995 · 190 citations

Rare Diseases, Variable Severity, Ophthalmology +6

Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus

Élodie Bal, Lekbir Baala, Céline Cluzeau et al. · Human Mutation · 2007 · 103 citations

Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.

Norma B. Romero, F.M.S. Tomé, France Leturcq et al. · PubMed · 1994 · 40 citations

Rare Diseases, Serum Creatine Kinase, Mendelian Disorder +12

Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

Aziza Sbiti, F. El Kerch, Abdelaziz Sefiani · BioMed Research International · 2002 · 32 citations · Full text

Urology, Mendelian Disorder, Exon Deletions +13

Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa.

F. El Kerch, Abdelaziz Sefiani, K. Azibi et al. · Journal of Medical Genetics · 1994 · 30 citations · Full text

Genetics, Genetic Epidemiology, Linkage Analysis +20