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Genetic Testing|December 17, 2008
Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan populationOmar Abidi, Redouane Boulouiz, Halima Nahili, et al.
Legal Medicine (Tokyo, Japan)|April 30, 2013
Mutation rate at 17 Y-STR loci in "Father/Son" pairs from moroccan populationAdil Laouina, Sellama Nadifi, Redouane Boulouiz, et al.
Molecular Vision|October 26, 2007
Analysis of MYO7A in a Moroccan family with Usher syndrome type 1B: novel loss-of-function mutation and non-pathogenicity of p.Y1719CRedouane Boulouiz, Yun Li, Omar Abidi, et al.
Biochemical and Biophysical Research Communications|March 3, 2012
Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing lossMajida Charif, Omar Abidi, Redouane Boulouiz, et al.
Clinical Biochemistry|November 8, 2024
Carrier frequency and molecular basis of hemoglobinopathies among blood donors in eastern Morocco: Implications for blood donation and genetic diagnosisIhab Belmokhtar, Karam Yahya Belmokhtar, Saida Lhousni, et al.
Biopreservation and Biobanking|March 26, 2020
Patients' Knowledge and Attitude Toward Biobanks in Eastern MoroccoSaida Lhousni, Fatiha Daoudi, Ihab Belmokhtar, et al.
Biochemical Genetics|June 6, 2014
Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysisHouda Benrahma, Hicham Charoute, Khaled Lasram, et al.
Human Heredity|January 24, 2021
Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan FamilySoukaina Elrharchi, Zied Riahi, Sara Salime, et al.
International Journal of Pediatric Otorhinolaryngology|July 20, 2010
Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing lossHalima Nahili, Majida Charif, Redouane Boulouiz, et al.
Gene|April 18, 2013
Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing lossMajida Charif, Amina Bakhchane, Omar Abidi, et al.
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