Publications by authors named "Imen Chelly"

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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment.
Rahma Mkaouar, Zied Riahi, Cherine Charfeddine, Imen Chelly, Hela Boudabbous

PLoS One· November 2021

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Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients.
Mediha Trabelsi, Malek Nouira, Faouzi Maazoul, Lilia Kraoua, Rim Meddeb, Imen Chelly

Int J Pediatr Otorhinolaryngol· December 2017

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Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategy.
Mediha Trabelsi, Imen Chelly, Faouzi Maazoul, Myriam Chaabouni, Ines Ouertani

Eur J Med Genet· January 2013

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Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case report.
Lilia Kraoua, Myriam Chaabouni, Elisabeth Ewers, Imen Chelly, Ines Ouertani

Eur J Med Genet· October 2011

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

Mol Vis· April 2010

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