检索结果 - Alrohaif, Hadil

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    Whole-exome sequencing identifies mutations in MYMK in a mild form of Carey-Fineman-Ziter syndrome

    Whole-exome sequencing identifies mutations in MYMK in a mild form of Carey-Fineman-Ziter syndrome 由 Alrohaif, Hadil, Töpf, Ana, Evangelista, Teresinha, Lek, Monkol, McArthur, Daniel, Lochmüller, Hanns

    出版 2018
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    Case Report: The Genetic Diagnosis of Duchenne Muscular Dystrophy in the Middle East

    Case Report: The Genetic Diagnosis of Duchenne Muscular Dystrophy in the Middle East 由 Alghamdi, Fouad, Al-Tawari, Asmaa, Alrohaif, Hadil, Alshuaibi, Walaa, Mansour, Hicham, Aartsma-Rus, Annemieke, Mégarbané, André

    出版 2021
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