Publications by authors named "Lamia Cherif"

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Identification of a novel mutation in FOXL2 gene that leads to blepharophimosis ptosis epicanthus inversus and telecanthus syndrome in a Tunisian consanguineous family.
Ibtissem Chouchene, Kaouthar Derouiche, Afif Chaabouni, Lamia Cherif, Ahlem Amouri

Genet Test Mol Biomarkersยท February 2010

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