Hasil Pencarian - Najumuddin
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Case report: A novel de novo loss of function variant in the DNA-binding domain of TBX2 causes severe osteochondrodysplasia oleh Misbahuddin M. Rafeeq, Hussam Aly Sayed Murad, Najumuddin, Samee Ullah, Zaheer Ahmed, Qamre Alam, Muhammad Bilal, Alaa Hamed Habib, Ziaullah M. Sain, Muhammad Jawad Khan, Muhammad Umair, Muhammad Umair
Diterbitkan 2023-01-01
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Whole exome sequencing identified five novel variants in CNTN2, CARS2, ARSA, and CLCN4 leading to epilepsy in consanguineous families oleh Angham Abdulrhman Abdulkareem, Angham Abdulrhman Abdulkareem, Qaiser Zaman, Qaiser Zaman, Qaiser Zaman, Hamza Khan, Sabar Khan, Gauhar Rehman, Nabeel Tariq, Mashal Ahmad, Muhammad Owais, Najumuddin, Osama Yousef Muthaffar, Fehmida Bibi, Fehmida Bibi, Rin Khang, Seung Woo Ryu, Muhammad Imran Naseer, Muhammad Imran Naseer, Musharraf Jelani
Diterbitkan 2023-06-01
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