Hasil Pencarian - Mohamed Taoudi

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  1. 1
    Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report

    Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report oleh Najlae Adadi, Maryem Sahli, Grégory Egéa, Ilham Ratbi, Mohamed Taoudi, Layla Zniber, Wafaa Jdioui, Said El Mouatassim, Abdelaziz Sefiani

    Diterbitkan 2018-10-01
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  2. 2
    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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  3. 3
    Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease

    Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease oleh Abdelali Zrhidri, Saadia Amasdl, Jaber Lyahyai, Hanane Elouardi, Bouchra Chkirate, Laure Raymond, Grégory Egéa, Mohamed Taoudi, Said El Mouatassim, Abdelaziz Sefiani

    Diterbitkan 2017-09-01
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