Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human gene von Chograni, M, Alahdal, H M, Rejili, M

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Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family von Chograni, M., Alkuraya, F.S., Ourteni, I., Maazoul, F., Lariani, I., Chaabouni, H.B.

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RGS6: a novel gene associated with congenital cataract, mental retardation, and microcephaly in a Tunisian family von Chograni, Manèl, Alkuraya, Fowzan S, Maazoul, Faouzi, Lariani, Imen, Chaabouni-Bouhamed, Habiba

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Absence of PITX3 mutation in a Tunisian family with congenital cataract and mental retardation von Chograni, Manèl, Chaabouni, Myriam, Chelly, Imen, Helayem, Mohamed Bechir, Chaabouni-Bouhamed, Habiba

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Genetic diversity and population structure among Rosmarinus officinalis L. (Lamiaceae) varieties: var. typicus Batt. and var. troglodytorum Maire. based on multiple traits von Zaouali, Y., Chograni, H., Trimech, R., Boussaid, M.

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Genetic diversity and chemical polymorphism of Tunisian Lavandula multifida L. (Lamiaceae) populations von Chograni, H, Zaouali, Y, Boussaid, M

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51 TVT colposuspension without preoperative urodynamic studies von Sadig, A., Manunta, A., Chograni, S., Kabbaj, M., Bensalah, K., Vincendeau, S., Patard, J.J., Lobel, B.

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