De Novo Balanced Translocation t (7;16) (p22.1; p11.2) Associated with Autistic Disorder

por Bayou, Nadia, M'rad, Ridha, Belhaj, Ahlem, Daoud, Hussein, Ben Jemaa, Lamia, Zemni, Ramzi, Briault, Sylvain, Helayem, M. Bechir, Chaabouni, Habiba
Publicado 2008

The Creatine Transporter Gene Paralogous at 16p11.2 Is Expressed in Human Brain

por Bayou, Nadia, M’rad, Ridha, Belhaj, Ahlem, Daoud, Hussein, Zemni, Ramzi, Briault, Sylvain, Helayem, M. Béchir, Ben Jemaa, Lamia, Chaabouni, Habiba
Publicado 2008

New familial cases of karyomegalic interstitial nephritis with mutations in the FAN1 gene

por Rejeb, Imen, Jerbi, Mouna, Jilani, Houweyda, Gaied, Hanène, Elaribi, Yasmina, Hizem, Syrine, Aoudia, Raja, Hedri, Hafedh, Zaied, Chiraz, Abid, Salwa, Bacha, Hassen, BenAbdallah, Taieb, BenJemaa, Lamia, Goucha, Rim
Publicado 2021

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

por Sassi, Hela, Elaribi, Yasmina, Jilani, Houweyda, Rejeb, Imen, Hizem, Syrine, Sebai, Molka, Kasdallah, Nadia, Bouthour, Habib, Hannachi, Samia, Beygo, Jasmin, Saad, Ali, Buiting, Karin, H’mida Ben‐Brahim, Dorra, BenJemaa, Lamia
Publicado 2021