Nadifi S - Search Results

1

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.

Weil D, El-Amraoui A, Masmoudi S, Mustapha M, Kikkawa Y, Lainé S, Delmaghani S, Adato A, Nadifi S, Zina ZB, Hamel C, Gal A, Ayadi H, Yonekawa H, Petit C. Weil D, et al. Among authors: nadifi s. Hum Mol Genet. 2003 Mar 1;12(5):463-71. doi: 10.1093/hmg/ddg051. Hum Mol Genet. 2003. PMID: 12588794

2

Autosomal recessive and sporadic deafness in Morocco: high frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant.

Gazzaz B, Weil D, Raïs L, Akhyat O, Azeddoug H, Nadifi S. Gazzaz B, et al. Among authors: nadifi s. Hear Res. 2005 Dec;210(1-2):80-4. doi: 10.1016/j.heares.2005.08.001. Epub 2005 Oct 21. Hear Res. 2005. PMID: 16243461

3

The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population.

Dieterich K, Zouari R, Harbuz R, Vialard F, Martinez D, Bellayou H, Prisant N, Zoghmar A, Guichaoua MR, Koscinski I, Kharouf M, Noruzinia M, Nadifi S, Sefiani A, Lornage J, Zahi M, Viville S, Sèle B, Jouk PS, Jacob MC, Escalier D, Nikas Y, Hennebicq S, Lunardi J, Ray PF. Dieterich K, et al. Among authors: nadifi s. Hum Mol Genet. 2009 Apr 1;18(7):1301-9. doi: 10.1093/hmg/ddp029. Epub 2009 Jan 15. Hum Mol Genet. 2009. PMID: 19147683

4

A haplotype-linked four base pair deletion upstream of the A gamma globin gene coincides with decreased gene expression.

Beldjord C, Ducrocq R, Nadifi S, Lapoumeroulie C, Elion J, Labie D. Beldjord C, et al. Among authors: nadifi s. Hum Genet. 1992 Aug;89(6):625-8. doi: 10.1007/BF00221951. Hum Genet. 1992. PMID: 1355067

5

Nucleotide sequence evidence of the unicentric origin of the beta C mutation in Africa.

Trabuchet G, Elion J, Dunda O, Lapouméroulie C, Ducrocq R, Nadifi S, Zohoun I, Chaventre A, Carnevale P, Nagel RL, et al. Trabuchet G, et al. Among authors: nadifi s. Hum Genet. 1991 Sep;87(5):597-601. doi: 10.1007/BF00209020. Hum Genet. 1991. PMID: 1680789

6

Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss.

Bakhchane A, Bousfiha A, Charoute H, Salime S, Detsouli M, Snoussi K, Nadifi S, Kabine M, Rouba H, Dehbi H, Roky R, Charif M, Barakat A. Bakhchane A, et al. Among authors: nadifi s. Eur J Med Genet. 2016 Jun;59(6-7):325-9. doi: 10.1016/j.ejmg.2016.05.002. Epub 2016 May 8. Eur J Med Genet. 2016. PMID: 27169813

7

A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco.

Belmouden A, Melki R, Hamdani M, Zaghloul K, Amraoui A, Nadifi S, Akhayat O, Garchon HJ. Belmouden A, et al. Among authors: nadifi s. Clin Genet. 2002 Oct;62(4):334-9. doi: 10.1034/j.1399-0004.2002.620415.x. Clin Genet. 2002. PMID: 12372064

8

Population genetic data of eight tetrameric short tandem repeats (STRs) in Casablanca resident population to use in forensic casework.

Chbel F, Nadifi S, Martinez-Bouzas C, Louahlia S, Azeddoug H, Martinez De Pancorbo M. Chbel F, et al. Among authors: nadifi s. Forensic Sci Int. 2003 Mar 12;132(1):82-3. doi: 10.1016/s0379-0738(02)00433-4. Forensic Sci Int. 2003. PMID: 12689756

9

[Polymorphism of six Alu-insertions in residents of Morocco: comparative study in Arab and Berber populations and residents of Casablanca].

Chbel F, de Pancorbo MM, Martinez-Bouzas C, Azeddoug H, Alvarez-Alvarez M, Rodriguez-Tojo MJ, Nadifi S. Chbel F, et al. Among authors: nadifi s. Genetika. 2003 Oct;39(10):1398-405. Genetika. 2003. PMID: 14658345 Russian.

10

Duchenne and Becker muscular dystrophy: contribution of a molecular and immunohistochemical analysis in diagnosis in Morocco.

Bellayou H, Hamzi K, Rafai MA, Karkouri M, Slassi I, Azeddoug H, Nadifi S. Bellayou H, et al. Among authors: nadifi s. J Biomed Biotechnol. 2009;2009:325210. doi: 10.1155/2009/325210. Epub 2009 May 19. J Biomed Biotechnol. 2009. PMID: 19461958 Free PMC article.

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