Two Infants with Beckwith-Wiedemann Syndrome by Ratbi I, Elalaoui S, Sefiani A

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MYH Associated Polyposis with a p.Tyr165Cys Mutation in a Moroccan Patient by Laarabi F, Jaouad I, El Kerch F, Sefiani A

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Ankyloblepharon-ectodermal defects-cleft lip-palate syndrome due to a novel missense mutation in the SAM domain of the TP63 gene by Tajir M, Lyahyai J, Guaoua S, El Alloussi M, Sefiani A

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Misdiagnosis of Tracher-Collins Syndrome Initially Attributed to Drug Teratogenicity: A Moroccan Case Report by Lamzouri A, EL Rherbi A, Ratbi I, Laarabi FZ, Chahboune R, Elalaoui SC, Hamdaoui H, Bencheikh RS, Sefiani A

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Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicism. by Twigg, S, Ousager, L, Miller, K, Zhou, Y, Elalaoui, S, Sefiani, A, Bak, G, Hove, H, Hansen, L, Fagerberg, C, Tajir, M, Wilkie, A