F. El Kerch - Concepedia

Author

F. El Kerch

Also Known As

EL KERCH, F., F E el Kerch, F El Kerch, F el Kerch, F. El Kerch, Fatiha El Kerch

Publications

442

Citations

H-Index

Concepts

All Affiliations

F. El Kerch is an author at Institut National d'Hygiène du Maroc specializing in medicine, pathology, and genetics.

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	292
2	Pathology	3	3	102
3	Public Health	1	1	30
4	Molecular Genetics	1	1	30
5	Molecular Medicine	1	1	32

F. El Kerch

Publications

419

Citations

H-Index

Page 1

	Year	Citations
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity Fédérica Piccolo, Steven L. Roberds, Marc Jeanpierre, Nature Genetics Rare DiseasesVariable SeverityOphthalmologyPrimary AdhalinopathyDegenerative Disease	1995	190
Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus Élodie Bal, Lekbir Baala, Céline Cluzeau, Human Mutation	2007	103
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, PubMed Rare DiseasesSerum Creatine KinaseMendelian DisorderGenetic DisorderGenetics	1994	40
Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients Aziza Sbiti, F. El Kerch, Abdelaziz Sefiani BioMed Research International UrologyMendelian DisorderExon DeletionsDmd GeneMedicine	2002	32
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, Journal of Medical Genetics GeneticsGenetic EpidemiologyLinkage AnalysisPathologyGenetic Homogeneity	1994	30
Carrier Frequency of the c.525delT Mutation in the <i>SGCG</i> Gene and Estimated Prevalence of Limb Girdle Muscular Dystrophy Type 2C Among the Moroccan Population F. El Kerch, Ilham Ratbi, Aziza Sbiti, Genetic Testing and Molecular Biomarkers	2014	24

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