Search Results - Maria Mansouri

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  1. 1

    1p36 deletion syndrome: first case report in Morocco detected by fluorescence in situ hybridization (FISH): a case report by Kenza Dafir, Fatima Zahra Bouzid, Maria Mansouri, Nisrine Aboussair

    Published in The Pan African Medical Journal (2020-12-01)
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  2. 2

    Focal Dermal Hypoplasia: Case Series by Maria Mansouri, Fatima Zohra Bouzid, Said Amal, Oufae Hocar, Nissrine Aboussair

    Published in Indian Journal of Dermatology (2023-01-01)
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  3. 3

    Clinical and Radiological Aspects of Pycnodysostosis: 1st Series of the Genetics Department of the Mohammed VI University Hospital of Marrakech by Kenza Dafir, Fatima Zahrae Bouzid, Maria Mansouri, Hassan Akallakh, Imane Ait Sab, Mohammed Bouskraoui, Nisrine Aboussair

    Published in Journal of Medical Sciences and Health (2023-12-01)
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  4. 4

    Associations between clinical characteristics and angiotensin-converting enzyme gene insertion/deletion polymorphism in Moroccan population with Type-2 diabetic nephropathy by Maria Mansouri, Amal Zniber, Lamia Boualla, Ghizlane El Badaoui, Mariam Benkacem, Kaoutar Rifai, Abdelmjid Chraibi, Loubna Benamar, Abdelaziz Sefiani, Rabia Bayahia

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  5. 5

    Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report by Jaber Lyahyai, Bouchra Ouled Amar Bencheikh, Siham C. Elalaoui, Maria Mansouri, Lamia Boualla, Alexandre DIonne-Laporte, Dan Spiegelman, Patrick A. Dion, Patrick Cossette, Guy A. Rouleau, Abdelaziz Sefiani

    Published in BMC Pediatrics (2018-02-01)
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