Search Results - Nweder, Mohamad Sayah

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  1. 1
    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

    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 Moassas, Faten, Nweder, Mohamad Sayah, Murad, Hossam

    Published in BMC pediatrics
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  2. 2
    Molecular analysis of the AGXT gene in Syrian patients suspected with primary hyperoxaluria type 1

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

    Published in BMC medical genomics
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  3. 3
    Hb Knossos (HBB: c.82G T), [beta]-globin CD 5 (-CT) (HBB: c.17_18delCT) and [delta]-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with [beta]-thalassemia intermedia

    Hb Knossos (HBB: c.82G T), [beta]-globin CD 5 (-CT) (HBB: c.17_18delCT) and [delta]-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with [beta]-thalassemia interme... by Murad, Hossam, Moassas, Faten, Nweder, Mohamad Sayah

    Published in BMC pediatrics
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  4. 4
    Hb Knossos mutations in a Syrian patient with [beta]-thalassemia intermedia

    Hb Knossos mutations in a Syrian patient with [beta]-thalassemia intermedia by Moassas, Faten, Nweder, Mohamad Sayah, Murad, Hossam

    Published in BMC pediatrics
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  5. 5
    Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss

    Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss by Moassass, Faten, Al-Halabi, Bassel, Nweder, Mohamad Sayah, Al-Achkar, Walid

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