Chafik A - Search Results

1

GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.

Abidi O, Boulouiz R, Nahili H, Ridal M, Alami MN, Tlili A, Rouba H, Masmoudi S, Chafik A, Hassar M, Barakat A. Abidi O, et al. Among authors: chafik a. Int J Pediatr Otorhinolaryngol. 2007 Aug;71(8):1239-45. doi: 10.1016/j.ijporl.2007.04.019. Epub 2007 Jun 5. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17553572

2

Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness.

Nahili H, Ridal M, Boulouiz R, Abidi O, Imken L, Rouba H, Alami MN, Chafik A, Hassar M, Barakat A. Nahili H, et al. Among authors: chafik a. Int J Pediatr Otorhinolaryngol. 2008 Nov;72(11):1633-6. doi: 10.1016/j.ijporl.2008.07.015. Epub 2008 Sep 21. Int J Pediatr Otorhinolaryngol. 2008. PMID: 18809214

3

The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population.

Abidi O, Boulouiz R, Nahili H, Imken L, Rouba H, Chafik A, Barakat A. Abidi O, et al. Among authors: chafik a. Biochem Biophys Res Commun. 2008 Dec 19;377(3):971-4. doi: 10.1016/j.bbrc.2008.10.086. Epub 2008 Oct 24. Biochem Biophys Res Commun. 2008. PMID: 18952066

4

Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.

Abidi O, Boulouiz R, Nahili H, Bakhouch K, Wakrim L, Rouba H, Chafik A, Hassar M, Barakat A. Abidi O, et al. Among authors: chafik a. Genet Test. 2008 Dec;12(4):569-74. doi: 10.1089/gte.2008.0063. Genet Test. 2008. PMID: 19072567

5

Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.

Nahili H, Charif M, Boulouiz R, Bounaceur S, Benrahma H, Abidi O, Chafik A, Rouba H, Kandil M, Barakat A. Nahili H, et al. Among authors: chafik a. Int J Pediatr Otorhinolaryngol. 2010 Sep;74(9):1071-4. doi: 10.1016/j.ijporl.2010.06.008. Epub 2010 Jul 15. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20637512

6

Novel mutations involving the INSL3 gene associated with cryptorchidism.

El Houate B, Rouba H, Sibai H, Barakat A, Chafik A, Chadli el B, Imken L, Bogatcheva NV, Feng S, Agoulnik AI, McElreavey K. El Houate B, et al. Among authors: chafik a. J Urol. 2007 May;177(5):1947-51. doi: 10.1016/j.juro.2007.01.002. J Urol. 2007. PMID: 17437853

7

AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men.

Imken L, El Houate B, Chafik A, Nahili H, Boulouiz R, Abidi O, Chadli E, Louanjli N, Elfath A, Hassar M, McElreavey K, Barakat A, Rouba H. Imken L, et al. Among authors: chafik a. Asian J Androl. 2007 Sep;9(5):674-8. doi: 10.1111/j.1745-7262.2007.00290.x. Asian J Androl. 2007. PMID: 17712485 Free article.

8

Analysis of MYO7A in a Moroccan family with Usher syndrome type 1B: novel loss-of-function mutation and non-pathogenicity of p.Y1719C.

Boulouiz R, Li Y, Abidi O, Bolz H, Chafik A, Kubisch C, Roub H, Wollnik B, Barakat A. Boulouiz R, et al. Among authors: chafik a. Mol Vis. 2007 Oct 2;13:1862-5. Mol Vis. 2007. PMID: 17960123

9

No association between T222P/LGR8 mutation and cryptorchidism in the Moroccan population.

El Houate B, Rouba H, Imken L, Sibai H, Chafik A, Boulouiz R, Chadli E, Hassar M, McElreavey K, Barakat A. El Houate B, et al. Among authors: chafik a. Horm Res. 2008;70(4):236-9. doi: 10.1159/000151596. Epub 2008 Sep 5. Horm Res. 2008. PMID: 18772597

10

A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family.

Boulouiz R, Li Y, Soualhine H, Abidi O, Chafik A, Nürnberg G, Becker C, Nürnberg P, Kubisch C, Wollnik B, Barakat A. Boulouiz R, et al. Among authors: chafik a. Am J Med Genet A. 2008 Dec 1;146A(23):3086-9. doi: 10.1002/ajmg.a.32525. Am J Med Genet A. 2008. PMID: 18973245 No abstract available.

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