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Unveiling the heritability of selected unexplored pharmacogenetic markers in the Saudi population by Mohammad A. Alshabeeb, Mohammad A. Alshabeeb, Deemah Alwadaani, Deemah Alwadaani, Sireen A. R. Shilbayeh, Fatemah A. Alherz, Ali Alghubayshi, Ali Alghubayshi
Published 2025-05-01Get full text
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Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome) by Majid Alfadhel, Bashayr S. Alhubayshi, Muhammad Umair, Ahmed Alfaidi, Deemah Alwadaani, Essra Aloyouni, Safdar Abbas, Abdulkareem Al Abdulrahman, Mohammed Aldrees, Abeer Al Tuwaijri, Ruaa S. Alharithy, Abdulaziz Alajlan, Abdulrahman Alswaid, Saad Almohrij, Sultan Al-Khenaizan
Published 2025-01-01Get full text
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