about
Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophreniaThe schizophrenia phenotype in 22q11 deletion syndromeMolecular mechanisms in 22q11 deletion syndrome.Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndromeCopy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse modelThe 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in miceSchizophrenia and 22q11.2 deletion syndrome.Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.Velo-Cardio-Facial Syndrome.Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India.The importance of understanding cognitive trajectories: the case of 22q11.2 deletion syndrome.Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory.Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome.Phenotype of adults with the 22q11 deletion syndrome: A review22q11 deletion syndrome: a genetic subtype of schizophrenia.Finding schizophrenia genes.Chromosomal abnormalities and schizophrenia.Mouse Models of 22q11.2-Associated Autism Spectrum DisorderGenome-wide approaches to schizophrenia.Genetic insights into schizophreniaA multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.The genetics of schizophrenia and bipolar disorder: dissecting psychosisSchizophrenia and genetics: new insights.Keratoconus in an adult with 22q11.2 deletion syndromeExtracardiac 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 schizophreniaPostmaturity in a genetic subtype of schizophrenia22q11.2 deletion status and disease burden in children and adolescents with tetralogy of Fallot.A novel SNP in COMT is associated with alcohol dependence but not opiate or nicotine dependence: a case control studyQualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia.Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome.The behavioural phenotype in velo-cardio-facial syndrome.Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disordersAlterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brainAnnotation: velo-cardio-facial syndrome.Assessment of parental disclosure of a 22q11.2 deletion syndrome diagnosis and implications for clinicians.
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
22q11 deletion syndrome in adults with schizophrenia.
@ast
22q11 deletion syndrome in adults with schizophrenia.
@en
type
label
22q11 deletion syndrome in adults with schizophrenia.
@ast
22q11 deletion syndrome in adults with schizophrenia.
@en
prefLabel
22q11 deletion syndrome in adults with schizophrenia.
@ast
22q11 deletion syndrome in adults with schizophrenia.
@en
P2093
P2860
P1476
22q11 deletion syndrome in adults with schizophrenia.
@en
P2093
A S Bassett
K Hodgkinson
R Weksberg
P2860
P304
P356
10.1002/(SICI)1096-8628(19980710)81:4<328::AID-AJMG10>3.3.CO;2-8
P577
1998-07-01T00:00:00Z