A Newly-Discovered Mutation in the RFX6 Gene of the Rare Mitchell-Riley Syndrome

por Khan, Nusrat, Dandan, Waleed, Al Hassani, Noura, Hadi, Suha
Publicado 2016

A novel missense heterozygous mutation in MAP3K1 gene causes 46, XY disorder of sex development: case report and literature review

por Al Shamsi, Aisha, Al Hassani, Noura, Hamchou, Moustafa, Almazrouei, Raya, Mhanni, Aziz
Publicado 2020

Patients' Perception of the Use of the EasyPod™ Growth Hormone Injector Device and Impact on Injection Adherence: A Multi-Center Regional Study

por Deeb, Asma, Al Yaarubi, Saif, Abbas, Bassam Bin, Al Jubeh, Jamal, Chaturvedi, Deepti, Al Hassani, Noura, Mutair, Angham, Al Masri, Neamat, Al Sanad, Yazan, Al Shidhani, Azza, Mahmoud, Noha Samir, Alherbish, Abdullah, Savage, Martin O.
Publicado 2022