Unraveling the Complexity of Apert Syndrome: Genetics, Clinical Insights, and Future Frontiers

por Kumari, Kajol, Saleh, Inam, Taslim, Sanzida, Ahmad, Sana, Hussain, Iqbal, Munir, Zainab, Javed, Tamleel, Virk, Muhammad Furqan Ismat, Javed, Saleha, Bisharat, Pakeezah, Ur Rehman, Ubaid
Publicado 2023

The Impact of Artificial Intelligence on Optimizing Diagnosis and Treatment Plans for Rare Genetic Disorders

por Abdallah, Shenouda, Sharifa, Mouhammad, I.KH. Almadhoun, Mohammed Khaleel, Khawar, Muhammad Muneeb, Shaikh, Unzla, Balabel, Khaled M, Saleh, Inam, Manzoor, Amima, Mandal, Arun Kumar, Ekomwereren, Osatohanmwen, Khine, Wai Mon, Oyelaja, Oluwaseyi T.
Publicado 2023