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Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome?

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Year: 2012
Type: review
Source: Current Opinion in Neurology
DOI: 10.1097/wco.0b013e328352dd58
Authors: Kate Baker, Jacob A.S. Vorstman
Institutions: University of Cambridge, University Medical Center Utrecht
Language: English

Topic: Genomic variations and chromosomal abnormalities
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: Wellcome Trust, National Institute for Health and Care Research, National Institutes of Health
Award: G2018255794
OpenAlex ID: W2008954066
FWCI: 1.185
Cites: 62
Cited by: 64
Related to: 10
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