Hasil Pencarian - Mohamed Taoudi
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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 2018-07-01Dapatkan teks lengkap
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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 2017-09-01Dapatkan teks lengkap
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