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

por Moassas, Faten, Nweder, Mohamad Sayah, Murad, Hossam
Publicado 2019

Molecular analysis of the AGXT gene in Syrian patients suspected with primary hyperoxaluria type 1

por Murad, Hossam, Alhalabi, Mohamad Baseel, Dabboul, Amir, Alfakseh, Nour, Nweder, Mohamad Sayah, Zghib, Youssef, Wannous, Hala
Publicado 2021