M'HAMDI Oussama, OUERTANI Ines

Update on the Genetics of Bardet-Biedl Syndrome, Molecular Syndromology, vol. 5, N° 2, Février 2014

M'HAMDI Oussama, OUERTANI Ines, MAAZOUL Faouzi, M'RAD Ridha

Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis, Clinical Genetics, vol. 85, N° 2, Juin 2014

RIAHI Awatef, KHARRAT Maher

High-resolution melting HRM assay for the detection of recurrent BRCA1/BRCA2 germline mutations in Tunisian breast/ovarian cancer families, Familial Cancer, vol. 13, N° 4, Décembre 2014

TRIFI CHOGRANI Manel, OUERTANI Ines, MAAZOUL Faouzi

Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family, Clinical Genetics, vol. n, N° n, Octobre 2014

TRIFI CHOGRANI Manel

Molecular analysis of the PAX6 gene for aniridia and congenital cataracts in Tunisian families, Human Genome Variation, vol. n, N° n, Octobre 2014

M'RAD Ridha

Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutations, Genetic Testing and Molecular Biomarkers, vol. 18, N° 11, Novembre 2014