Joma, R., Radwan, S., Hannoun, S., Hasson, J., & Aiesh, B. M. (2025). Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome identified by whole-exome sequencing (WES): A case report from a developing country. Oxford Medical Case Reports, 2025(6), 1. https://doi.org/10.1093/omcr/omaf079
Chicago Style (17th ed.) CitationJoma, Rahaf, Shahed Radwan, Sakhaa Hannoun, Jawad Hasson, and Banan M. Aiesh. "Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome Identified by Whole-exome Sequencing (WES): A Case Report from a Developing Country." Oxford Medical Case Reports 2025, no. 6 (2025): 1. https://doi.org/10.1093/omcr/omaf079.
MLA (9th ed.) CitationJoma, Rahaf, et al. "Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome Identified by Whole-exome Sequencing (WES): A Case Report from a Developing Country." Oxford Medical Case Reports, vol. 2025, no. 6, 2025, p. 1, https://doi.org/10.1093/omcr/omaf079.