Dorra H'mida Ben-Brahim

Partial KCNQ1OT1 hypomethylation: A disguised familial Beckwith–Wiedemann syndrome as a sporadic adrenocortical tumor

M. Gribaa, A. Zakhama, A. Saâd, 2014, Applied & translational genomics.

Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature

J. Beygo, A. Saâd, K. Buiting, 2021, Molecular genetics & genomic medicine.