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Biomolecules & Biomedicine|February 12, 2026
<i>DYSF </i>gene variant spectrum in Arab populations across eight countries: A systematic reviewFatimazahra Smaili, Khawla Zerrouki, Fatima Ezzahra Aouni, et al.
Pediatric Endocrinology Reviews : PER|December 18, 2018
Ellis-Van Creveld Syndrome and Dandy-Walker Malformation: An Uncommon AssociationKhadija Boujtat, Siham Rouf, Imane Boutahar, et al.
The Pan African Medical Journal|February 26, 2024
[Williams-Beuren syndrome: a retrospective study of a series of 11 cases at the Mohammed VI University Hospital in Marrakech]Fatima Zahrae Bouzid, Hanane Ait Hammou, Hassan Akallakh, et al.
Gene|January 29, 2013
Germline mosaicism in Rubinstein-Taybi syndromeMariam Tajir, Patricia Fergelot, Guenaelle Lancelot, et al.
Genetic Testing and Molecular Biomarkers|April 19, 2012
Frequency of IL28B rs12979860 single-nucleotide polymorphism alleles in newborn infants and in patients with chronic hepatitis C in MoroccoMariam Tajir, Mustapha Elmachad, Nawal Kabbaj, et al.
European Journal of Medical Genetics|July 7, 2012
Pyruvate dehydrogenase deficiency caused by a new mutation of PDHX gene in two Moroccan patientsMariam Tajir, Jean Baptiste Arnoux, Audrey Boutron, et al.
Annales De Biologie Clinique|July 21, 2023
[Contribution of cytogenetic in the diagnosis of Edwards's syndrome: about 9 cases]Fatima Ezzahra Aouni, Khawla Zerrouki, Fatimazahra Smaili, et al.
ACG Case Reports Journal|November 4, 2024
Granulomatous Colitis Due to Hermansky-Pudlak SyndromeHajar Koulali, Samira Azzmouri, Mariam Tajir, et al.
Biopreservation and Biobanking|March 26, 2020
Patients' Knowledge and Attitude Toward Biobanks in Eastern MoroccoSaida Lhousni, Fatiha Daoudi, Ihab Belmokhtar, et al.
African Health Sciences|November 19, 2021
Clinical description and mutational profile of a Moroccan series of patients with Rubinstein Taybi syndromeSiham Chafai Elalaoui, Wiam Smaili, Julien Van-Gils, et al.
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