Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome - Wikidata - wikimedia - TriplyDB

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

http://www.wikidata.org/entity/Q33622905

about

Behavioural phenotypes and special educational needs: is aetiology important in the classroom?The genetics of autistic disorders and its clinical relevance: a review of the literature High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome Genomics and autism spectrum disorder Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome The effect of hypocalcemia in early childhood on autism-related social and communication skills in patients with 22q11 deletion syndrome Copy 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 model Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice Proline affects brain function in 22q11DS children with the low activity COMT 158 allele Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.Evidence for involvement of GNB1L in autism.Analysis of TBX1 variation in patients with psychotic and affective disorders.22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases Proline and COMT status affect visual connectivity in children with 22q11.2 deletion syndrome.The NRG1 exon 11 missense variant is not associated with autism in the Central Valley of Costa Rica.Velo-Cardio-Facial Syndrome.Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory.Cortical interneurons require Jnk1 to enter and navigate the developing cerebral cortex.Examining the Overlap between Autism Spectrum Disorder and 22q11.2 Deletion Syndrome.Mouse Models of 22q11.2-Associated Autism Spectrum Disorder Co-occurrence of ADHD and autism spectrum disorders: phenomenology and treatment.Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders.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.Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?Childhood and current autistic features in adolescents with schizotypal personality disorder.An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome Complexity of a small non-protein coding sequence in chromosomal region 22q11.2: presence of specialized DNA secondary structures and RNA exon/intron motifs.Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.Association testing of copy number variants in schizophrenia and autism spectrum disorders.Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome.Assessment of parental disclosure of a 22q11.2 deletion syndrome diagnosis and implications for clinicians.

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Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

http://www.wikidata.org/entity/Q33622905

description

2005 nî lūn-bûn

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2005 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2005 թվականի օգոստոսին հրատարակված գիտական հոդված

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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Autism spectrum disorders and ...... rmed 22q11.2 deletion syndrome

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Autism spectrum disorders and ...... rmed 22q11.2 deletion syndrome

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Autism spectrum disorders and ...... rmed 22q11.2 deletion syndrome

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Autism spectrum disorders and ...... rmed 22q11.2 deletion syndrome

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Autism spectrum disorders and ...... rmed 22q11.2 deletion syndrome

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Journal of Autism and Developmental Disorders

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Autism spectrum disorders and ...... rmed 22q11.2 deletion syndrome

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Alison Weissman

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Beverly S Emanuel

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Elaine H Zackai

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Jennifer Pinto-Martin

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Marsha Gerdes

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Sarah E Fine

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P2860

Broader autism phenotype: evidence from a family history study of multiple-incidence autism families

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

The Philadelphia story: the 22q11.2 deletion: report on 250 patients

A case-control family history study of autism

The epidemiology of Asperger syndrome. A total population study

Autistic symptoms among children and young adults with isodicentric chromosome 15

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.

Prevalence of 22q11 microdeletion.

The epidemiology of autism: a review.

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4

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Donna M McDonald-McGinn

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7627162

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16134031

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Autism spectrum

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2814423

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