Ngā hua rapu - Al-Sayed, Moeen

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  1. 1
    Novel mutations underlying argininosuccinic aciduria in Saudi Arabia

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

    I whakaputaina 2010
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  2. 2
    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) mā Alsmadi, Osama, Meyer, Brian F, Alkuraya, Fowzan, Wakil, Salma, Alkayal, Fadi, Al-Saud, Haya, Ramzan, Khushnooda, Al-Sayed, MoeenAldeen

    I whakaputaina 2009
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  3. 3
    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 mā Al-Hassnan, Zuhair N., Khalifa, Ola A., Bubshait, Dalal K., Tulbah, Sahar, Alkorashy, Maarab, Alzaidan, Hamad, Alowain, Mohammed, Rahbeeni, Zuhair, Al-Sayed, Moeen

    I whakaputaina 2018
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