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International Journal of Pediatric Otorhinolaryngology|September 24, 2008
Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafnessHalima Nahili, Mohamed Ridal, Redouane Boulouiz, et al.
Hormone Research|September 6, 2008
No association between T222P/LGR8 mutation and cryptorchidism in the Moroccan populationBrahim El Houate, Hassan Rouba, Laila Imken, et al.
Indian Journal of Human Genetics|December 17, 2013
Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing lossMajida Charif, Redouane Boulouiz, Amina Bakhechane, et al.
International Journal of Pediatric Otorhinolaryngology|June 8, 2007
GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutationOmar Abidi, Redouane Boulouiz, Halima Nahili, et al.
Molecular Genetics & Genomic Medicine|May 26, 2022
Molecular heterogeneity of β-thalassemia variants in the Eastern region of MoroccoIhab Belmokhtar, Saida Lhousni, Mounia Elidrissi Errahhali, et al.
Asian Journal of Andrology|August 23, 2007
AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan menLaila Imken, Brahim El Houate, Abdelaziz Chafik, 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.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 10, 2026
Identification of Novel and Known Variants in Epigenetic Genes Associated with Syndromic 46,XY Differences of Sex Development among Moroccan PatientsImane Cherkaoui, Saida Lhousni, Manal Elidrissi Errahhali, et al.
Journal of Community Health|March 29, 2011
Maternal effect and familial aggregation in a type 2 diabetic Moroccan populationHouda Benrahma, Imen Arfa, Majida Charif, et al.
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