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Article

Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion Syndrome

16 Sept 2015

Abstract excerpt

22q11.2 Deletion syndrome (22q11.2DS) is a chromosomal microdeletion that affects approximately 40 to 50 genes and affects various organs and systems throughout the body. Detection is typically achieved by fluorescence in situ hybridization after diagnosis of one of the major features of the deletion or via chromosomal microarray or noninvasive prenatal testing. The physical phenotype can include congenital heart...

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PMID: 26372046
DOI: 10.1097/dbp.0000000000000210

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