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

por H'mida Ben-Brahim, Dorra, Hammami, Sabeur, Haddaji Mastouri, Marwa, Trabelsi, Saoussen, Chourabi, Maroua, Sassi, Sihem, Mougou, Soumaya, Gribaa, Moez, Zakhama, Abdelfattah, Guédiche, Mohamed Neji, Saad, Ali
Publicado 2014