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Community Genetics|August 12, 2008
Tunisia: communities and community geneticsHabiba Chaabouni-BouhamedFamilial Cancer|July 30, 2014
High-resolution melting (HRM) assay for the detection of recurrent BRCA1/BRCA2 germline mutations in Tunisian breast/ovarian cancer familiesAouatef Riahi, Maher Kharrat, Imen Lariani, et al.Journal of Community Genetics|November 24, 2011
Prevalence of Bardet-Biedl syndrome in TunisiaOussama M'hamdi, Ines Ouertani, Faouzi Maazoul, et al.Journal of Biosocial Science|January 30, 2015
CONSANGUINITY AND HOMOZYGOSITY AMONG TUNISIAN PATIENTS WITH AN AUTOSOMAL RECESSIVE DISORDERWided Kelmemi, Imene Chelly, Maher Kharrat, et al.Breast Cancer (Tokyo, Japan)|March 31, 2016
Family history predictors of BRCA1/BRCA2 mutation status among Tunisian breast/ovarian cancer familiesAouatef Riahi, Mohamel El Ghourabi, Asma Fourati, et al.Human Genome Variation|April 16, 2016
Molecular analysis of the PAX6 gene for aniridia and congenital cataracts in Tunisian familiesManèl Chograni, Kaouther Derouiche, Myriam Chaabouni, et al.La Tunisie Medicale|May 11, 2011
Non-syndromic autosomal recessive mental retardation in Tunisian families : exclusion of GRIK2 and TUSC3 genesOussama Mhamdi, Maher Kharrat, Ridha Mrad, et al.La Tunisie Medicale|May 11, 2011
[Linkage analysis of six Algerian families with autosomal recessive non specific mental retardation]Nadia Guessibia, Noureddine Sarrai, Nassima Methari, et al.European Journal of Human Genetics : EJHG|May 12, 2011
The first missense mutation of NHS gene in a Tunisian family with clinical features of NHS syndrome including cardiac anomalyManèl Chograni, Imen Rejeb, Lamia Ben Jemaa, et al.Investigative Ophthalmology & Visual Science|December 20, 2014
RGS6: a novel gene associated with congenital cataract, mental retardation, and microcephaly in a Tunisian familyManèl Chograni, Fowzan S Alkuraya, Faouzi Maazoul, et al.Pageof 2