Hasil Pencarian - Imane Cherkaoui Jaouad

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  1. 1
    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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  2. 2
    First application of next-generation sequencing in four families with Wilson disease in Morocco

    First application of next-generation sequencing in four families with Wilson disease in Morocco oleh Maryem Sahli, Abdelali Zrhidri, Youssef El Kadiri, Imane Cherkaoui Jaouad, Toufik Meskini, Abdelaziz Sefiani

    Diterbitkan 2023-09-01
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  3. 3
    Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: a case report

    Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: a case report oleh Maryem Sahli, Abdelali Zrhidri, Imad Boualaoui, Imane Cherkaoui Jaouad, Youssef El Kadiri, Yassine Nouini, Abdelaziz Sefiani

    Diterbitkan 2023-09-01
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  4. 4
    A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report

    A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report oleh Imane Cherkaoui Jaouad, Abdelali Zrhidri, Wafaa Jdioui, Jaber Lyahyai, Laure Raymond, Grégory Egéa, Mohamed Taoudi, Said El Mouatassim, Abdelaziz Sefiani

    Diterbitkan 2018-07-01
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  5. 5
    Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report

    Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report oleh Yahya Benbouchta, Imane Cherkaoui Jaouad, Habiba Tazi, Hamza Elorch, Mouna Ouhenach, Abdelali Zrhidri, Khalid Sadki, Abdelaziz Sefiani, Jaber Lyahyai, Amina Berraho

    Diterbitkan 2021-01-01
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  6. 6
    Early diagnosis of congenital muscular pathologies using next-generation sequencing: experiences from a tertiary center in Morocco

    Early diagnosis of congenital muscular pathologies using next-generation sequencing: experiences from a tertiary center in Morocco oleh Youssef El Kadiri, Ilham Ratbi, Mouna Ouhenach, Siham Chafai Elalaoui, Imane Cherkaoui Jaouad, Abdelali Zrhidri, Maryem Sahli, Nazha Birouk, Abdelaziz Sefiani, Jaber Lyahyai

    Diterbitkan 2023-05-01
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