Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
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Genetic Syndromes associated with Congenital Heart DiseaseConverging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndromeBehavioral and Psychiatric Phenotypes in 22q11.2 Deletion SyndromeChromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complicationsCopy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.Factors affecting articulation skills in children with velocardiofacial syndrome and children with cleft palate or velopharyngeal dysfunction: a preliminary report.Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in miceEvidence for involvement of GNB1L in autism.22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive casesFeasibility and preliminary efficacy data from a computerized cognitive intervention in children with chromosome 22q11.2 deletion syndrome.Cognitive characteristics of children with genetic syndromes.A new account of the neurocognitive foundations of impairments in space, time and number processing in children with chromosome 22q11.2 deletion syndrome.Associations between performance on the Rey-Osterrieth Complex Figure and regional brain volumes in children with and without velocardiofacial syndrome.Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22qThe importance of understanding cognitive trajectories: the case of 22q11.2 deletion syndrome.Mapping cortical thickness in children with 22q11.2 deletions.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.Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome.CHARGE (coloboma, heart defect, atresia choanae, retarded growth and development, genital hypoplasia, ear anomalies/deafness) syndrome and chromosome 22q11.2 deletion syndrome: a comparison of immunologic and nonimmunologic phenotypic features.Mouse Models of 22q11.2-Associated Autism Spectrum DisorderIncreased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome.Discrepancies in parent and teacher ratings of social-behavioral functioning of children with chromosome 22q11.2 deletion syndrome: implications for assessment.Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: a 3-year follow-up study.22q11.2 deletion syndrome: are motor deficits more than expected for IQ level?Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counselingPrenatal diagnosis of the 22q11.2 deletion syndrome.Taking advantage of early diagnosis: preschool children with the 22q11.2 deletion.A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.Is child intelligence associated with parent and sibling intelligence in individuals with developmental disorders? An investigation in youth with 22q11.2 deletion (velo-cardio-facial) syndrome.Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome.Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype?Developmental malformation of the corpus callosum: a review of typical callosal development and examples of developmental disorders with callosal involvement.Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome
P2860
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P2860
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
@en
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
@nl
type
label
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
@en
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
@nl
prefLabel
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
@en
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
@nl
P2093
P1476
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
@en
P2093
Batshaw ML
Driscoll DA
Emanuel BS
McDonald-McGinn DM
P304
P356
10.1016/S0022-3476(99)70415-4
P407
P577
1999-02-01T00:00:00Z