Autor: Hanan Aljedani
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A rare case of de novo 20p12.3 microdeletion syndrome in a nine-year-old female: case report and literature review
Chromosomal deletion syndromes are common worldwide. However, one rare condition that distinguishes a limited number of reported cases and variable phenotypes is 20p12.3 microdeletion syndrome. This case report describes a nine-year-old girl diagnosed …