Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
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.
African Health Sciences|August 8, 2025
JAK2 mutational status and the contribution of TERT and JAK2 polymorphisms to the occurrence of myeloproliferative neoplasms in Eastern MoroccoKaram Yahya Belmokhtar, Mounia Elidrissi Errahhali, Saida Lhousni, et al.
American Journal of Human Genetics|February 23, 2010
Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing lossYun Li, Esther Pohl, Redouane Boulouiz, 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.
American Journal of Human Genetics|October 23, 2012
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing lossSimon von Ameln, Geng Wang, Redouane Boulouiz, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2023
Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disordersFranziska Langhammer, Reza Maroofian, Rueda Badar, et al.
Pageof 4