Rebai A - Search Results

1

Further evidence of the clinical and genetic heterogeneity of recessive transgressive PPK in the Mediterranean region.

Charfeddine C, Mokni M, Kassar S, Zribi H, Bouchlaka C, Boubaker S, Rebai A, Ben Osman A, Abdelhak S. Charfeddine C, et al. Among authors: rebai a. J Hum Genet. 2006;51(10):841-845. doi: 10.1007/s10038-006-0002-8. Epub 2006 Jul 25. J Hum Genet. 2006. PMID: 16865292

2

Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.

Bouchlaka C, Abdelhak S, Amouri A, Ben Abid H, Hadiji S, Frikha M, Ben Othman T, Amri F, Ayadi H, Hachicha M, Rebaï A, Saad A, Dellagi K; Tunisian Fanconi Anemia Study Group. Bouchlaka C, et al. Among authors: rebai a. J Hum Genet. 2003;48(7):352-61. doi: 10.1007/s10038-003-0037-z. Epub 2003 Jun 24. J Hum Genet. 2003. PMID: 12827451

3

Allelic structure and distribution of 103 STR loci in a Southern Tunisian population.

Maalej A, Rebai A, Ayadi A, Jouida J, Makni H, Ayadi H. Maalej A, et al. Among authors: rebai a. J Genet. 2004 Apr;83(1):65-71. doi: 10.1007/BF02715830. J Genet. 2004. PMID: 15240910

4

Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.

Masmoudi S, Charfedine I, Rebeh IB, Rebai A, Tlili A, Ghorbel AM, Belguith H, Petit C, Drira M, Ayadi H. Masmoudi S, et al. Among authors: rebai a. Clin Genet. 2004 Oct;66(4):358-64. doi: 10.1111/j.1399-0004.2004.00311.x. Clin Genet. 2004. PMID: 15355440

5

Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients.

Bouchlaka C, Maktouf C, Mahjoub B, Ayadi A, Sfar MT, Sioud M, Gueddich N, Belhadjali Z, Rebaï A, Abdelhak S, Dellagi K. Bouchlaka C, et al. Among authors: rebai a. J Hum Genet. 2007;52(3):262-270. doi: 10.1007/s10038-007-0110-0. Epub 2007 Feb 7. J Hum Genet. 2007. PMID: 17285242

6

Sample size computation for association studies using case-parents design.

Kharrat N, Ayadi I, Rebaï A. Kharrat N, et al. Among authors: rebai a. J Genet. 2006 Dec;85(3):187-91. doi: 10.1007/BF02935329. J Genet. 2006. PMID: 17406092 No abstract available.

7

Lack of association between the angiotensin-converting enzyme gene (I/D) polymorphism and diabetic nephropathy in Tunisian type 2 diabetic patients.

Arfa I, Abid A, Nouira S, Elloumi-Zghal H, Malouche D, Mannai I, Zorgati MM, Ben Alaya N, Rebai A, Zouari B, Ben Ammar S, Ben Rayana MC, Hmida S, Blousa-Chabchoub S, Abdelhak S. Arfa I, et al. Among authors: rebai a. J Renin Angiotensin Aldosterone Syst. 2008 Mar;9(1):32-6. doi: 10.3317/jraas.2008.002. J Renin Angiotensin Aldosterone Syst. 2008. PMID: 18404607 Free article.

8

Haplotypic classification of dystrophic epidermolysis bullosa in Tunisian consanguineous families: implication for diagnosis.

Ouragini H, Cherif F, Daoud W, Kassar S, Charfeddine C, Rebaï A, Boubaker S, Ben Osman-Dhahri A, Abdelhak S. Ouragini H, et al. Among authors: rebai a. Arch Dermatol Res. 2008 Aug;300(7):365-70. doi: 10.1007/s00403-008-0861-2. Epub 2008 May 22. Arch Dermatol Res. 2008. PMID: 18496702

9

Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.

Hmani-Aifa M, Benzina Z, Zulfiqar F, Dhouib H, Shahzadi A, Ghorbel A, Rebaï A, Söderkvist P, Riazuddin S, Kimberling WJ, Ayadi H. Hmani-Aifa M, et al. Among authors: rebai a. Eur J Hum Genet. 2009 Apr;17(4):474-82. doi: 10.1038/ejhg.2008.167. Epub 2008 Oct 15. Eur J Hum Genet. 2009. PMID: 18854872 Free PMC article.

10

Clinical, histological and genetic investigation of Buschke-Fischer-Brauer's disease in Tunisian families.

Bchetnia M, Charfeddine C, Kassar S, Hanchi I, Tounsi-Guettiti H, Rebai A, Osman AD, Kubisch C, Abdelhak S, Boubaker S, Mokni M. Bchetnia M, et al. Among authors: rebai a. J Dermatol Sci. 2009 Apr;54(1):54-6. doi: 10.1016/j.jdermsci.2008.11.008. Epub 2009 Jan 10. J Dermatol Sci. 2009. PMID: 19136236 No abstract available.

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