Developmental changes in multivariate neuroanatomical patterns that predict risk for psychosis in 22q11.2 deletion syndrome. [electronic resource]
Producer: 20110614Description: 322-31 p. digitalISSN:- 1879-1379
- Adolescent
- Analysis of Variance
- Brain -- pathology
- Brain Mapping
- Catechol O-Methyltransferase -- genetics
- Child
- Chromosome Deletion
- Chromosomes, Human, Pair 22 -- genetics
- Cognition Disorders -- diagnosis
- Developmental Disabilities -- genetics
- Female
- Functional Laterality
- Genome-Wide Association Study -- methods
- Genotype
- Humans
- Magnetic Resonance Imaging
- Male
- Neuropsychological Tests
- Predictive Value of Tests
- Psychiatric Status Rating Scales
- Psychotic Disorders -- complications
- Risk Factors
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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