Coexistence of 9p Deletion Syndrome and Autism Spectrum Disorder
Overview
Affiliations
Deletion or duplication of the short arm of chromosome 9 may lead to a variety of clinical conditions including craniofacial and limb abnormalities, skeletal malformations, mental retardation, and autism spectrum disorder. Here, we present a case report of 5-year-old boy with 9p deletion syndrome and autism spectrum disorder.
Using a new analytic approach for genotyping and phenotyping chromosome 9p deletion syndrome.
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