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Genetic Testing and Molecular Biomarkers|September 19, 2015
AGXT Gene Mutations and Prevalence of Primary Hyperoxaluria Type 1 in Moroccan PopulationLamiae Boualla, Mariam Tajir, Najat Oulahiane, et al.American Journal of Medical Genetics. Part A|September 20, 2012
An inherited LMNA gene mutation in atypical Progeria syndromeYassamine Doubaj, Annachiara De Sandre-Giovannoli, Esteves-Vieira Vera, et al.The Pan African Medical Journal|March 11, 2020
[Lung cancer in Eastern Morocco: where do we stand?]Karam Yahya Belmokhtar, Mariam Tajir, Redouane Boulouiz, et al.European Journal of Human Genetics : EJHG|October 16, 2014
Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinomaJean-Benoît Courcet, Siham Chafai Elalaoui, Laurence Duplomb, 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.Pageof 2