檢索結果 - Al-Sayed, Moeen

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    Novel mutations underlying argininosuccinic aciduria in Saudi Arabia

    Novel mutations underlying argininosuccinic aciduria in Saudi Arabia 由 Imtiaz, Faiqa, Al-Sayed, Moeen, Trabzuni, Danyah, Al-Mubarak, Bashair R, Alsmadi, Osama, Rashed, Mohamed S, Meyer, Brian F

    出版 2010
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    Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)

    Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3) 由 Alsmadi, Osama, Meyer, Brian F, Alkuraya, Fowzan, Wakil, Salma, Alkayal, Fadi, Al-Saud, Haya, Ramzan, Khushnooda, Al-Sayed, MoeenAldeen

    出版 2009
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    The phenotype, genotype, and outcome of infantile-onset Pompe disease in 18 Saudi patients

    The phenotype, genotype, and outcome of infantile-onset Pompe disease in 18 Saudi patients 由 Al-Hassnan, Zuhair N., Khalifa, Ola A., Bubshait, Dalal K., Tulbah, Sahar, Alkorashy, Maarab, Alzaidan, Hamad, Alowain, Mohammed, Rahbeeni, Zuhair, Al-Sayed, Moeen

    出版 2018
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