Search Results - Mohamad Sayah Nweder

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    Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia by Faten Moassas, Mohamad Sayah Nweder, Hossam Murad

    Published 2019
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  2. 2
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    Molecular analysis of the AGXT gene in Syrian patients suspected with primary hyperoxaluria type 1 by Hossam Murad, Mohamad Baseel Alhalabi, Amir Dabboul, Nour Alfakseh, Mohamad Sayah Nweder, Youssef Zghib, Hala Wannous

    Published 2021
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