Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism

por Mkaouar, Rahma, Abdallah, Lamia Cherif Ben, Naouali, Chokri, Lahbib, Saida, Turki, Zinet, Elouej, Sahar, Bouyacoub, Yosra, Somai, Maali, Mcelreavey, Kenneth, Bashamboo, Anu, Abdelhak, Sonia, Messaoud, Olfa
Publicado 2021

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