Hasil Pencarian - Wiam Smaili

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  1. 1
    A novel frameshift mutation in the XPC gene in a Moroccan patient: a case report

    A novel frameshift mutation in the XPC gene in a Moroccan patient: a case report oleh Yassamine Doubaj, Wiam Smaili, Fatima-Zahra Laarabi, Abdelaziz Sefiani

    Diterbitkan 2017-06-01
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  2. 2
    Application of next generation sequencing in genetic counseling a case of a couple at risk of cystinosis

    Application of next generation sequencing in genetic counseling a case of a couple at risk of cystinosis oleh Mouna Ouhenach, Abdelali Zrhidri, Imane Cherkaoui Jaouad, Wiam Smaili, Abdelaziz Sefiani

    Diterbitkan 2020-12-01
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  3. 3
    Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series

    Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series oleh Maryem Sahli, Abdelali Zrhidri, Siham Chafai Elaloui, Wiam Smaili, Jaber Lyahyai, Fatima Zohra Oudghiri, Abdelaziz Sefiani

    Diterbitkan 2019-08-01
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