Hasil Pencarian - Bouchaïb Gazzaz

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  1. 1
    A novel variant of unknown significance in pediatric epilepsy: a case report

    A novel variant of unknown significance in pediatric epilepsy: a case report oleh Wafaa Bouzroud, Amal Tazzite, Ikhlass Boussakri, Bouchaïb Gazzaz, Hind Dehbi

    Diterbitkan 2023-07-01
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  2. 2
    R306X Mutation in the Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report

    R306X Mutation in the Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report oleh Wafaa Bouzroud, Amal Tazzite, Sarah Berrada, Bouchaïb Gazzaz, Hind Dehbi

    Diterbitkan 2022-09-01
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  3. 3
    Complement Factor I deficiency: A novel homozygous gene mutation

    Complement Factor I deficiency: A novel homozygous gene mutation oleh Wafaa Bouzroud, Amal Tazzite, Ibenbrahim yousra, Bouchaïb Gazzaz, Hind Dehbi

    Diterbitkan 2022-06-01
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  4. 4
    Anthropogenetic study of the Arabic - speaking population of Chaouia Ouardigha (Morocco) based on autosomal STRs

    Anthropogenetic study of the Arabic - speaking population of Chaouia Ouardigha (Morocco) based on autosomal STRs oleh Othmane Essoubaiy, Bouchaïb Gazzaz, Hakima Yahia, Hicham EL Ossmani, Jalal Talbi, Brahim El Houate, Taoufiq Fechtali

    Diterbitkan 2024-04-01
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