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Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome identified by whole-exome sequencing (WES): a case report from a developing country.

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Bibliographic Details
Title:	Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome identified by whole-exome sequencing (WES): a case report from a developing country.
Authors:	Joma, Rahaf¹ (AUTHOR), Radwan, Shahed¹ (AUTHOR), Hannoun, Sakhaa² (AUTHOR), Hasson, Jawad³ (AUTHOR), Aiesh, Banan M⁴ (AUTHOR)
Source:	Oxford Medical Case Reports. Jun2025, Vol. 2025 Issue 6, p1-3. 3p.
Database:	Academic Search Ultimate
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Description
ISSN:	20538855
DOI:	10.1093/omcr/omaf079