Clinical and genetic aspects of the 15q11.2 BP1 –BP2 microdeletion disorder

ConclusionsThe summarised results indicate that chromosome 15q11.2 BP1–BP2 microdeletion is emerging as one of the most common cytogenetic abnormalities seen in individuals with intellectual impairment, autism spectrum disorder and other related behavioural or clinical findings, but more research is needed.
Source: Journal of Intellectual Disability Research - Category: Disability Authors: Tags: Original Manuscript Source Type: research