Canlyniadau Chwilio - Alrohaif, Hadil

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  1. 1
    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 gan Alrohaif, Hadil, Töpf, Ana, Evangelista, Teresinha, Lek, Monkol, McArthur, Daniel, Lochmüller, Hanns

    Cyhoeddwyd 2018
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    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  2. 2
    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 gan Alghamdi, Fouad, Al-Tawari, Asmaa, Alrohaif, Hadil, Alshuaibi, Walaa, Mansour, Hicham, Aartsma-Rus, Annemieke, Mégarbané, André

    Cyhoeddwyd 2021
    Cael y testun llawn Cael y testun llawn Cael y testun llawn
    Text
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:

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