Hasil Pencarian - 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

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

    Diterbitkan 2020-12-01
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  2. 2
    Focal Dermal Hypoplasia: Case Series

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

    Diterbitkan 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

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

    Diterbitkan 2023-12-01
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  4. 4
    Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family

    Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family oleh Fatima Zahra Bouzid, Maria Mansouri, Chaikhy Abdelaziz, Nisrine Louhab, Sablonniere Bernard, Isabelle Strubi-vuillaume, Kenza Dafir, Nisrine Aboussair

    Diterbitkan 2021-02-01
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  5. 5
    Associations between clinical characteristics and angiotensin-converting enzyme gene insertion/deletion polymorphism in Moroccan population with Type-2 diabetic nephropathy

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

    Diterbitkan 2017-01-01
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  6. 6
    Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

    Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report oleh 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

    Diterbitkan 2018-04-01
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  7. 7
    Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

    Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report oleh 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

    Diterbitkan 2018-02-01
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