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Jouali F, El Haddoumi G, Antra I, Benhida R, Ben Itto A, Fekkak J. A Case Report: Identification of a Pathogenic Microdeletion at Chromosome 21q21.3q22.13 Using Whole-Exome Sequencing and CNV Analysis in a Moroccan Child with Global Developmental Delay. Genes. 2025; 16(11):1280. https://doi.org/10.3390/genes16111280

Jouali, Farah, Ghyzlane El Haddoumi, Imane Antra, Rachid Benhida, Afaf Ben Itto, and Jamal Fekkak. 2025. "A Case Report: Identification of a Pathogenic Microdeletion at Chromosome 21q21.3q22.13 Using Whole-Exome Sequencing and CNV Analysis in a Moroccan Child with Global Developmental Delay" Genes 16, no. 11: 1280. https://doi.org/10.3390/genes16111280

Jouali, F., El Haddoumi, G., Antra, I., Benhida, R., Ben Itto, A., & Fekkak, J. (2025). A Case Report: Identification of a Pathogenic Microdeletion at Chromosome 21q21.3q22.13 Using Whole-Exome Sequencing and CNV Analysis in a Moroccan Child with Global Developmental Delay. Genes, 16(11), 1280. https://doi.org/10.3390/genes16111280