22q11 deletion syndrome: a genetic subtype of schizophrenia.
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The schizophrenia phenotype in 22q11 deletion syndromeConverging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndromeReduced fronto-temporal and limbic connectivity in the 22q11.2 deletion syndrome: vulnerability markers for developing schizophrenia?Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit developmentChromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complicationsSequence diversity of KIAA0027/MLC1: are megalencephalic leukoencephalopathy and schizophrenia allelic disorders?Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes.Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome.Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal studyGenetics of schizophrenia: from animal models to clinical studiesAnalysis of TBX1 variation in patients with psychotic and affective disorders.Schizophrenia and abnormal brain network hubs.Schizophrenia and 22q11.2 deletion syndrome.Low platelet count in a 22q11 deletion syndrome subtype of schizophrenia.Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndromeA comprehensive analysis of 22q11 gene expression in the developing and adult brain.Phenotype of adults with the 22q11 deletion syndrome: A reviewNeurobehavioral evidence for changes in dopamine system activity during adolescence.Schizophrenia-Related Microdeletion Impairs Emotional Memory through MicroRNA-Dependent Disruption of Thalamic Inputs to the Amygdala.SlgA, encoded by the homolog of the human schizophrenia-associated gene PRODH, acts in clock neurons to regulate Drosophila aggressionChromosomal abnormalities and schizophrenia.Supportive evidence for reduced expression of GNB1L in schizophrenia.Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome.Genetic counselling for schizophrenia in the era of molecular genetics.Genetic insights into schizophreniaA multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.Schizophrenia: neural mechanisms for novel therapiesHow might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndromeSchizophrenia and genetics: new insights.Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.Clinically detectable copy number variations in a Canadian catchment population of schizophrenia.Dermatoglyphic profile in 22q deletion syndromeElevated rates of schizophrenia in a familial sample with mental illness and intellectual disabilityGenomic copy number variation in disorders of cognitive development.Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease.Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome.Patterns of dysmorphic features in schizophrenia
P2860
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P2860
22q11 deletion syndrome: a genetic subtype of schizophrenia.
description
1999 nî lūn-bûn
@nan
1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
22q11 deletion syndrome: a genetic subtype of schizophrenia.
@ast
22q11 deletion syndrome: a genetic subtype of schizophrenia.
@en
type
label
22q11 deletion syndrome: a genetic subtype of schizophrenia.
@ast
22q11 deletion syndrome: a genetic subtype of schizophrenia.
@en
prefLabel
22q11 deletion syndrome: a genetic subtype of schizophrenia.
@ast
22q11 deletion syndrome: a genetic subtype of schizophrenia.
@en
P2860
P1476
22q11 deletion syndrome: a genetic subtype of schizophrenia.
@en
P2093
P2860
P304
P356
10.1016/S0006-3223(99)00114-6
P407
P577
1999-10-01T00:00:00Z