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

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

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

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

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

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Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report von El Amrani, Zhour, Natiq, Abdelhafid, Sbiti, Aziza, Ratbi, Ilham, Liehr, Thomas, Sefiani, Abdelaziz, Sahli, Maryem

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Molecular diagnosis of dystrophinopathies in Morocco and report of six novel mutations von EL Kadiri, Youssef, Selouani, Yassir, Ratbi, Ilham, Lyahyai, Jaber, Zrhidri, Abdelali, Sahli, Maryem, Ouhenach, Mouna, Jaouad, Imane Cherkaoui, Sefiani, Abdelaziz, Sbiti, Aziza

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Smoking and associated factors among school teenagers in the city of Sousse (Smoking and school teenagers) von Limam, Manel, Marzouki, Maryem, El Ghardallou, Mariem, Sahli, Jihène, Ajmi, Thouraya, Zedini, Chekib

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