Showing results (1-10 of 14) with videos related to
Sort By:
Pageof 2
The Pan African Medical Journal|March 19, 2021
1p36 deletion syndrome: first case report in Morocco detected by fluorescence in situ hybridizationKenza Dafir, Fatima Zahra Bouzid, Maria Mansouri, et al.Indian Journal of Dermatology|May 8, 2023
Focal Dermal Hypoplasia: Case SeriesMaria Mansouri, Fatima Zohra Bouzid, Said Amal, et al.American Journal of Medical Genetics. Part A|July 7, 2016
Further evidence of POP1 mutations as the cause of anauxetic dysplasiaSiham Chafai Elalaoui, Fatima Zahra Laarabi, Maria Mansouri, et al.Journal of Medical Case Reports|November 7, 2015
A homozygous AHI1 gene mutation (p.Thr304AsnfsX6) in a consanguineous Moroccan family with Joubert syndrome: a case reportSiham Chafai-Elalaoui, Matthias Chalon, Nadia Elkhartoufi, et al.The Pan African Medical Journal|May 17, 2021
Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family (case report)Fatima Zahra Bouzid, Maria Mansouri, Chaikhy Abdelaziz, et al.Pediatric Neurology|December 3, 2014
A novel nonsense mutation in SCN9A in a Moroccan child with congenital insensitivity to painMaria Mansouri, Siham Chafai Elalaoui, Bouchra Ouled Amar Bencheikh, et al.Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|March 30, 2017
Associations between clinical characteristics and angiotensin-converting enzyme gene insertion/deletion polymorphism in Moroccan population with Type-2 diabetic nephropathyMaria Mansouri, Amal Zniber, Lamia Boualla, et al.American Journal of Medical Genetics. Part A|October 15, 2015
Novel DDR2 mutation identified by whole exome sequencing in a Moroccan patient with spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification typeMaria Mansouri, Hülya Kayserili, Siham Chafai Elalaoui, et al.African Health Sciences|July 8, 2024
Phenotypic and cytogenetic variability of patau syndrome in MoroccoHanane Ait Hammou, Mariam Sennaoui, Fatimazahra Bouzid, et al.OTO Open|June 30, 2026
Comprehensive Analysis and Genetic Insights Into GJB2 c.35delG Mutation-Associated Non-Syndromic Hearing Loss in MoroccoEl Mostafa Salman, Meriem El Qabli, Loubna Soufian, et al.Pageof 2