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Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi Arabia by Manal Alaamery, Manal Alaamery, Manal Alaamery, Salam Massadeh, Salam Massadeh, Salam Massadeh, Manar Aldarwish, Manar Aldarwish, Nour Albesher, Nour Albesher, Nora Aljawini, Othman Alahmed, Amna Kashgari, Amna Kashgari, Christopher A. Walsh, Wafaa Eyaid, Wafaa Eyaid
Published 2024-01-01
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Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish by Muhammad Umair, Muhammad Farooq Khan, Mohammed Aldrees, Marwan Nashabat, Kheloud M. Alhamoudi, Kheloud M. Alhamoudi, Muhammad Bilal, Yusra Alyafee, Abeer Al Tuwaijri, Manar Aldarwish, Ahmed Al-Rumayyan, Hamad Alkhalaf, Mohammad A. M. Wadaan, Majid Alfadhel, Majid Alfadhel
Published 2021-10-01
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