Double isochromosome X, A rare cytogenetic variant of turner syndrome: A case report and a review of the literature by Zerrouki K., Babakhouya A., Tajir M.

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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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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