Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review

por Khadija, Bochra, Rjiba, Khouloud, Dimassi, Sarra, Dahleb, Wafa, Kammoun, Molka, Hannechi, Hanen, Miladi, Najoua, Gouider-khouja, Neziha, Saad, Ali, Mougou-Zerelli, Soumaya
Publicado 2022

Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development

por Rjiba, Khouloud, Mougou-Zerelli, Soumaya, Hamida, Imen hadj, Saad, Ghada, Khadija, Bochra, Jelloul, Afef, Slimani, Wafa, Hasni, Yosra, Dimassi, Sarra, khelifa, Hela Ben, Sallem, Amira, Kammoun, Molka, Abdallah, Hamza Hadj, Gribaa, Moez, Bignon-Topalovic, Joelle, Chelly, Sami, Khairi, Hédi, Bibi, Mohamed, Kacem, Maha, Saad, Ali, Bashamboo, Anu, McElreavey, Kenneth
Publicado 2023