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, 1280.
https://doi.org/10.3390/genes16111280
AMA Style
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
Chicago/Turabian Style
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
APA Style
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
