Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysge...

por Rjiba, Khouloud, Slimani, Wafa, Gaddas, Meriem, Hassine, Ikbel Hadj, Jelloul, Afef, Khelifa, Hela Ben, El Amri, Fethi, Zaouali, Monia, Mcelreavey, Kenneth, Saad, Ali, Mougou-Zerelli, Soumaya
Publicado 2023

Molecular diagnosis of distal renal tubular acidosis in Tunisian patients: proposed algorithm for Northern Africa populations for the ATP6V1B1, ATP6V0A4 and SCL4A1 genes

por Elhayek, Donia, Perez de Nanclares, Gustavo, Chouchane, Slaheddine, Hamami, Saber, Mlika, Adnène, Troudi, Monia, Leban, Nadia, Ben Romdane, Wafa, Gueddiche, Mohamed Neji, El Amri, Féthi, Mrabet, Samir, Ben Chibani, Jemni, Castaño, Luis, Haj Khelil, Amel, Ariceta, Gema
Publicado 2013