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Page 1
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
Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene.
Ouechtati F, Merdassi A, Bouyacoub Y, Largueche L, Derouiche K, Ouragini H, Nouira S, Tiab L, Baklouti K, Rebai A, Schorderet DF, Munier FL, Zografos L, Abdelhak S, El Matri L. Ouechtati F, et al. Among authors: rebai a. J Hum Genet. 2011 Jan;56(1):22-8. doi: 10.1038/jhg.2010.128. Epub 2010 Nov 25. J Hum Genet. 2011. PMID: 21107338
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.
Evidence for association of the E23K variant of KCNJ11 gene with type 2 diabetes in Tunisian population: population-based study and meta-analysis.
Lasram K, Ben Halim N, Hsouna S, Kefi R, Arfa I, Ghazouani W, Jamoussi H, Benrahma H, Kharrat N, Rebai A, Ben Ammar S, Bahri S, Barakat A, Abid A, Abdelhak S. Lasram K, et al. Among authors: rebai a. Biomed Res Int. 2014;2014:265274. doi: 10.1155/2014/265274. Epub 2014 Jul 7. Biomed Res Int. 2014. PMID: 25165692 Free PMC article.
219 results