Genetic Disorders in Tunisia
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-05080-0_21
Reference116 articles.
1. Abdelmoula NB, Amouri A, Portnoi MF, Saad A, Boudawara T, Mhiri MN, Bahloul A, Rebai T (2004) Cytogenetics and fluorescence in situ hybridization assessment of sex-chromosome mosaicism in Klinefelter’s syndrome. Ann Genet 47:163–175
2. Aissi-Ben Moussa S, Moussa A, Lovecchio T, Kourda N, Najjar T, Ben Jilani S, El Gaaied A, Porchet N, Manai M, Buisine MP (2009) Identification and characterization of a novel MLH1 genomic rearrangement as the cause of HNPCC in a Tunisian family: evidence for a homologous Alu-mediated recombination. Fam Cancer 8:119–126
3. Al-Abdulkareem AA, Ballal SG (1998) Consanguineous marriage in an urban area of Saudi Arabia: rates and adverse health effects on the offspring. J Community Health 23:75–83
4. Al-Gazali LI, Bener A, Abdulrazzaq YM, Micallef R, al-Khayat AI, Gaber T (1997) Consanguineous marriages in the United Arab Emirates. J Biosoc Sci 29:491–497
5. Arfa I, Abid A, Malouche D, Ben Alaya N, Azegue TR, Mannai I, Zorgati MM, Ben Rayana MC, Ben Ammar S, Blousa-Chabchoub S, Ben Romdhane H, Zouari B, Dellagi MK, Abdelhak S (2007) Familial aggregation and excess maternal transmission of type 2 diabetes in Tunisia. Postgrad Med J 83:348–351
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1. Genetics and genomic medicine in Tunisia;Molecular Genetics & Genomic Medicine;2018-03
2. Distribution of allelic and genotypic frequencies of NAT2 and CYP2E1variants in Moroccan population;BMC Genetics;2014-12
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