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Consanguinity, endogamy, and genetic disorders in Tunisia.

Nizar Ben Halim , Nissaf Ben Alaya Bouafif , Lilia Romdhane , Rym Kefi Ben Atig , Ibtissem Chouchane , et al.
Journal of Community Genetics, 2013, 4 (2), pp.273-84. ⟨10.1007/s12687-012-0128-7⟩
Journal articles pasteur-00859212v1

Autism in Phenylketonuria Patients: From Clinical Presentation to Molecular Defects

Sameh Khemir , Soumaya Halayem , Hatem Azzouz , Hajer Siala , Maherzia Ferchichi , et al.
Journal of Child Neurology, 2016, 31 (7), pp.843--849. ⟨10.1177/0883073815623636⟩
Journal articles pasteur-01469443v1

Central areolar choroidal dystrophy associated with inherited drusen in a multigeneration Tunisian family: exclusion of the PRPH2 gene and the 17p13 locus

Farah Ouechtati , Olfa Belhadj Tahar , Amin Mhenni , Sonia Chakroun , Ibtissem Chouchene , et al.
Journal of Human Genetics, 2009, 54 (10), pp.589-594. ⟨10.1038/jhg.2009.82⟩
Journal articles pasteur-01375318v1