CNVxplorer: a web tool to assist clinical interpretation of CNVs in rare disease patients

por Requena, Francisco, Abdallah, Hamza Hadj, García, Alejandro, Nitschké, Patrick, Romana, Sergi, Malan, Valérie, Rausell, Antonio
Publicado 2021

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