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Frontiers in Genetics|March 11, 2024
A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literatureFatima Ouboukss, Zhour El Amrani, Hicham Bouchahta, et al.
Ophthalmic Genetics|June 6, 2022
Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disabilityZhour El Amrani, Siham Chafai Elalaoui, Wafae Jdioui, et al.
Genetic Testing and Molecular Biomarkers|April 18, 2012
Cytogenetic analysis of 5572 patients referred for suspected chromosomal abnormalities in MoroccoNisrine Aboussair, Imane Cherkaoui Jaouad, Souad Cherkaoui Dequaqui, et al.
Molecular Genetics & Genomic Medicine|February 26, 2026
Implementing a Tiered Genetic Testing Strategy for Muscular Dystrophies in Morocco: From Targeted Assays to Exome SequencingYasmina Rahmuni, Ilham Ratbi, Jaber Lyahyai, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 15, 2020
Molecular diagnosis of dystrophinopathies in Morocco and report of six novel mutationsYoussef El Kadiri, Yassir Selouani, Ilham Ratbi, et al.
The Pan African Medical Journal|August 23, 2021
Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemiaYassamine Doubaj, Abdelali Zrhidri, Siham Chafai Elalaoui, et al.
Nature Genetics|March 14, 2007
Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesisLekbir Baala, Sylvain Briault, Heather C Etchevers, et al.
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