Rouba H - Search Results

1

Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population.

Charoute H, Bakhchane A, Benrahma H, Romdhane L, Gabi K, Rouba H, Fakiri M, Abdelhak S, Lenaers G, Barakat A. Charoute H, et al. Among authors: rouba h. Hum Mutat. 2015 Nov;36(11):E2441-53. doi: 10.1002/humu.22835. Epub 2015 Jul 30. Hum Mutat. 2015. PMID: 26173767

2

Y-chromosome analysis in Egypt suggests a genetic regional continuity in Northeastern Africa.

Manni F, Leonardi P, Barakat A, Rouba H, Heyer E, Klintschar M, McElreavey K, Quintana-Murci L. Manni F, et al. Among authors: rouba h. Hum Biol. 2002 Oct;74(5):645-58. doi: 10.1353/hub.2002.0054. Hum Biol. 2002. PMID: 12495079

3

Y-chromosomal STR haplotypes in Berber and Arabic-speaking populations from Morocco.

Quintana-Murci L, Bigham A, Rouba H, Barakat A, McElreavey K, Hammer M. Quintana-Murci L, et al. Among authors: rouba h. Forensic Sci Int. 2004 Feb 10;140(1):113-5. doi: 10.1016/j.forsciint.2003.11.006. Forensic Sci Int. 2004. PMID: 15013173

4

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: rouba h. J Urol. 2007 May;177(5):1947-51. doi: 10.1016/j.juro.2007.01.002. J Urol. 2007. PMID: 17437853

5

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: rouba h. 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

6

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: rouba h. Horm Res. 2008;70(4):236-9. doi: 10.1159/000151596. Epub 2008 Sep 5. Horm Res. 2008. PMID: 18772597

7

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: rouba h. 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

8

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: rouba h. 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

9

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: rouba h. Genet Test. 2008 Dec;12(4):569-74. doi: 10.1089/gte.2008.0063. Genet Test. 2008. PMID: 19072567

10

Mutations in the protamine locus: association with spermatogenic failure?

Imken L, Rouba H, El Houate B, Louanjli N, Barakat A, Chafik A, McElreavey K. Imken L, et al. Among authors: rouba h. Mol Hum Reprod. 2009 Nov;15(11):733-8. doi: 10.1093/molehr/gap056. Epub 2009 Jul 14. Mol Hum Reprod. 2009. PMID: 19602509

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