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Molecular Syndromology|April 8, 2024
Triple-A Syndrome in Morocco: Founder Effect, Age Estimation of the <i>AAAS</i> c.1331+1G>A Variant, and Implications for Genetic DiagnosisKaram Yahya Belmokhtar, Imane Cherkaoui, Saida Lhousni, et al.
The Pan African Medical Journal|April 1, 2024
An overview of a preliminary multicenter retrospective study on food and drug allergies in Moroccan pediatric populationZakaria Zidane, Chaimaa Chahine, Karima Mohtadi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 23, 2024
First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism arrayManal Elidrissi Errahhali, Mounia Elidrissi Errahhali, Sara Ramdani, et al.
Molecular Syndromology|April 6, 2026
Identification of the Genetic Causes of Inherited Diseases in a North African Biobank: Implications for Genetic DiagnosisMajida Charif, Saida Lhousni, Ayad Ghanam, et al.
Clinics and Research in Hepatology and Gastroenterology|April 8, 2024
Phenotype and molecular characterization of Wilson's disease in MoroccoNadia Abbassi, Aicha Bourrahouat, Eduardo Couchonnal Bedoya, et al.
Biomed Research International|December 30, 2020
Morocco's First Biobank: Establishment, Ethical Issues, Biomedical Research Opportunities, and ChallengesSaida Lhousni, Karam Yahya Belmokhtar, Ihab Belmokhtar, et al.
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