Le diagnostic anténatal de la trisomie 21 par l'hybridation in situ en fluorescence (FISH): à propos des premiers tests réalisés au Maroc by Afaf Lamzouri, Abdelhafid Natiq, Mariam Tajir1, Mohamed Sendid, Abdelaziz Sefiani

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The Genetic Facets of Dravet Syndrome: Recent Insights by Hinde El Mouhi, Meriame Abbassi, Meryem Jalte, Abdelhafid Natiq, Laila Bouguenouch, Sana Chaouki

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Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myeloma by Hasna Hamdaoui, Abdelhafid Natiq, Oumaima Benlarroubia, Thomas Liehr, Hind Dehbi, Latifa Loukhmas, Fatima Chegdani

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A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature by Fatima Ouboukss, Fatima Ouboukss, Zhour El Amrani, Zhour El Amrani, Hicham Bouchahta, Ilham Ratbi, Aziza Sbiti, Thomas Liehr, Abdelaziz Sefiani, Abdelaziz Sefiani, Abdelhafid Natiq

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Clinical characterization of 72 patients with del(22)(q11.2q11.2) from different ethnic backgrounds by Luis A. Méndez-Rosado, Norma de León-Ojeda, Alina García, Frenny Sheth, Asmaa Gaadi, Ahmed Aziz Bousfiha, Mouna Lehlimi, Abdelhafid Natiq, Oxana S. Kurinnaia, Svetlana G. Vorsanova, Ivan Iourov, Dagmar Huhle, Thomas Liehr

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