A Mosaic PIK3CA Mutation in a Moroccan Female: Exploring the Diagnostic Challenges of PIK3CA-Related Overgrowth Spectrum

por Ahakoud, Mohamed, Daha Belghiti, Hanae, Ihlal, Hajar, Bouguenouch, Laila
Publicado 2023

A Case of Severe Teratozoospermia and Infertility Due to Homozygous Mutation c.144delC in the AURKC Gene

por Abbassi, Meriame, Sayel, Hanane, El Mouhi, Hinde, Jelte, Meryem, Ahakoud, Mohamed
Publicado 2023

Rare and Atypical Case of Turner Syndrome With Three Cell Lines

por Essouabni, Amal, Ahakoud, Mohamed, Aynaou, Hayat, Bouguenouch, Laila, Salhi, Houda, Karim, Ouldim, Elouahabi, Hanan
Publicado 2023

FLT3 Mutations in Acute Myeloid Leukemia: Unraveling the Molecular Mechanisms and Implications for Targeted Therapies

por Jalte, Meryem, Abbassi, Meriame, El Mouhi, Hinde, Daha Belghiti, Hanae, Ahakoud, Mohamed, Bekkari, Hicham
Publicado 2023

The Diagnosis and Genetic Mechanisms of Prader-Willi Syndrome: Findings From a Moroccan Population Study

por Ahakoud, Mohamed, Daha Belghiti, Hanae, Nedbour, Ayoub, Bouramtane, Abdelhamid, Chaouki, Sana, Bouguenouch, Laila, Ouldim, Karim
Publicado 2023