A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report von Cherkaoui Jaouad, Imane, Zrhidri, Abdelali, Jdioui, Wafaa, Lyahyai, Jaber, Raymond, Laure, Egéa, Grégory, Taoudi, Mohamed, El Mouatassim, Said, 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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A series of four patients with Sotos syndrome harboring novel NSD1 mutations: clinical and molecular description von Amllal, Nada, Zerkaoui, Maria, Jdioui, Wafaa, Elalaoui, Siham Chafai, Sefiani, Abdelaziz, Lyahyai, Jaber

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