(Q33622905)

28 July 2017

title

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

1 reference

28 July 2017

main subject

autism spectrum disorder

0 references

autism

0 references

author

Donna M McDonald-McGinn

6

object named as

Donna M McDonald-McGinn

1 reference

28 July 2017

Sarah E Fine

1

1 reference

28 July 2017

Alison Weissman

2

1 reference

28 July 2017

Marsha Gerdes

3

1 reference

28 July 2017

Jennifer Pinto-Martin

4

1 reference

28 July 2017

Elaine H Zackai

5

1 reference

28 July 2017

Beverly S Emanuel

7

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 August 2005

1 reference

Journal of Autism and Developmental Disorders

28 July 2017

published in

1 reference

28 July 2017

volume

35

1 reference

28 July 2017

issue

4

1 reference

28 July 2017

page(s)

461-470

1 reference

Epidemiological surveys of autism and other pervasive developmental disorders: an update

28 July 2017

cites work

1 reference

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21 June 2018

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21 June 2018

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Communication intervention for children with autism: a review of treatment efficacy

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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

21 June 2018

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Velo-cardio-facial syndrome: a distinctive behavioral phenotype

21 June 2018

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21 June 2018

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21 June 2018

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22q11 deletion syndrome: a genetic subtype of schizophrenia

21 June 2018

1 reference

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21 June 2018

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

21 June 2018

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

21 June 2018

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Autistic symptoms among children and young adults with isodicentric chromosome 15

21 June 2018

1 reference

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

21 June 2018

1 reference

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21 June 2018

1 reference

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21 June 2018

1 reference

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21 June 2018

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A case-control family history study of autism

21 June 2018

1 reference

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

21 June 2018

1 reference

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Autism and autistic-like conditions in Swedish rural and urban areas: a population study

21 June 2018

1 reference

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Autism under age 3 years: a clinical study of 28 cases referred for autistic symptoms in infancy

21 June 2018

1 reference

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Autism Diagnostic Interview-Revised and the Childhood Autism Rating Scale: convergence and discrepancy in diagnosing autism

21 June 2018

1 reference

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Genetics of childhood disorders: XLII. Autism, part 1: Diagnosis and assessment in autistic spectrum disorders

30 October 2018

1 reference

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Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects

30 October 2018

1 reference

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Neurological presentation of three patients with 22q11 deletion (CATCH 22 syndrome).

30 October 2018

1 reference

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The Modified Checklist for Autism in Toddlers: an initial study investigating the early detection of autism and pervasive developmental disorders

30 October 2018

1 reference

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Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2814423

Toward a developmental operational definition of autism

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2814423

The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: a family history study

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2814423

Prenatal and perinatal risk factors for autism

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2814423

Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria. IMGSAC. International Molecular Genetics Study of Autism Consortium

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2814423

Predictors of cognitive test patterns in autism families

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2814423

Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2814423

On cognitive variability in velocardiofacial syndrome: profound mental retardation and autism

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2814423

Parents and collateral relatives of children with pervasive developmental disorders: a family history study.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2814423

Empathy and cognition in high-functioning children with autism

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2814423

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16134031

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Velo-cardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16134031

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10803-005-5036-9

1 reference

Dimensions Publication ID

28 July 2017

0 references

1 reference

28 July 2017

1 reference