el Kerch FE - Search Results

1

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

Romero NB, Tomé FM, Leturcq F, el Kerch FE, Azibi K, Bachner L, Anderson RD, Roberds SL, Campbell KP, Fardeau M, et al. Romero NB, et al. Among authors: el kerch fe. C R Acad Sci III. 1994 Jan;317(1):70-6. C R Acad Sci III. 1994. PMID: 7987694

2

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

el Kerch F, Sefiani A, Azibi K, Boutaleb N, Yahyaoui M, Bentahila A, Vinet MC, Leturcq F, Bachner L, Beckmann J, et al. el Kerch F, et al. J Med Genet. 1994 Apr;31(4):342-3. doi: 10.1136/jmg.31.4.342. J Med Genet. 1994. PMID: 8071965 Free PMC article.

3

Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus.

Bal E, Baala L, Cluzeau C, El Kerch F, Ouldim K, Hadj-Rabia S, Bodemer C, Munnich A, Courtois G, Sefiani A, Smahi A. Bal E, et al. Hum Mutat. 2007 Jul;28(7):703-9. doi: 10.1002/humu.20500. Hum Mutat. 2007. PMID: 17354266

4

Carrier frequency of the c.525delT mutation in the SGCG gene and estimated prevalence of limb girdle muscular dystrophy type 2C among the Moroccan population.

El Kerch F, Ratbi I, Sbiti A, Laarabi FZ, Barkat A, Sefiani A. El Kerch F, et al. Genet Test Mol Biomarkers. 2014 Apr;18(4):253-6. doi: 10.1089/gtmb.2013.0326. Epub 2014 Feb 19. Genet Test Mol Biomarkers. 2014. PMID: 24552312 Free PMC article.

5

Cytogenetic and epidemiological profiles of Down syndrome in a Moroccan population: a report of 852 cases.

Jaouad IC, Cherkaoui Deqaqi S, Sbiti A, Natiq A, Elkerch F, Sefiani A. Jaouad IC, et al. Singapore Med J. 2010 Feb;51(2):133-6. Singapore Med J. 2010. PMID: 20358152 Free article.

6

[Confirmation of the high prevalence in Morocco of the homozygous mutation c.144delC in the aurora kinase C gene (AURKC) in the teratozoospermia with large-headed spermatozoa].

El Kerch F, Lamzouri A, Laarabi FZ, Zahi M, Ben Amar B, Sefiani A. El Kerch F, et al. J Gynecol Obstet Biol Reprod (Paris). 2011 Jun;40(4):329-33. doi: 10.1016/j.jgyn.2010.09.003. Epub 2011 Feb 24. J Gynecol Obstet Biol Reprod (Paris). 2011. PMID: 21353399 Free article. French.

7

Unexpected fertility and paternal UPD 22.

Ouldim K, Sbiti A, Natiq A, El-Kerch F, Cherkaoui S, Sefiani A. Ouldim K, et al. Fertil Steril. 2008 Nov;90(5):2013.e13-5. doi: 10.1016/j.fertnstert.2008.03.067. Epub 2008 Jun 20. Fertil Steril. 2008. PMID: 18571167 Free article.

8

Cytogenetic analysis of 5572 patients referred for suspected chromosomal abnormalities in Morocco.

Aboussair N, Jaouad IC, Dequaqui SC, Sbiti A, Elkerch F, Yahya B, Natiq A, Sefiani A. Aboussair N, et al. Genet Test Mol Biomarkers. 2012 Jun;16(6):569-73. doi: 10.1089/gtmb.2011.0265. Epub 2012 Apr 16. Genet Test Mol Biomarkers. 2012. PMID: 22506488

9

Non-association of Crohn's disease with NOD2 gene variants in Moroccan patients.

Hama I, Ratbi I, Reggoug S, Elkerch F, Kharrasse G, Errabih I, Ouazzani H, Sefiani A. Hama I, et al. Gene. 2012 May 10;499(1):121-3. doi: 10.1016/j.gene.2011.12.045. Epub 2012 Jan 14. Gene. 2012. PMID: 22266421

10

Frequencies of CYP3A5*1/*3 variants in a Moroccan population and effect on tacrolimus daily dose requirements in renal transplant patients.

Elmachad M, Elkabbaj D, Elkerch F, Laarabi FZ, Barkat A, Oualim Z, Sefiani A. Elmachad M, et al. Genet Test Mol Biomarkers. 2012 Jun;16(6):644-7. doi: 10.1089/gtmb.2011.0240. Epub 2012 Feb 3. Genet Test Mol Biomarkers. 2012. PMID: 22304537

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