Autism, language and communication in children with sex chromosome trisomies (Q35238891)

7 August 2017

title

Autism, language and communication in children with sex chromosome trisomies (English)

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7 August 2017

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Kate Nation

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14

Gaia Scerif

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author name string

Patricia A Jacobs

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Katherine Lachlan

3

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Diana Wellesley

4

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7 August 2017

Angela Barnicoat

5

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7 August 2017

Patricia A Boyd

6

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7 August 2017

Alan Fryer

7

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Prisca Middlemiss

8

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Sarah Smithson

9

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Kay Metcalfe

10

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Deborah Shears

11

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7 August 2017

Victoria Leggett

12

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Gaia Scerif

14

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7 August 2017

language of work or name

English

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publication date

23 July 2010

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Archives of Disease in Childhood

7 August 2017

published in

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7 August 2017

volume

96

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7 August 2017

issue

10

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7 August 2017

page(s)

954-959

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Genomic sister-disorders of neurodevelopment: an evolutionary approach

7 August 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Advances in autism genetics: on the threshold of a new neurobiology

13 July 2018

1 reference

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Autism and diagnostic substitution: evidence from a study of adults with a history of developmental language disorder

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Structural variation of chromosomes in autism spectrum disorder

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Association between microdeletion and microduplication at 16p11.2 and autism

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Is the prevalence of Klinefelter syndrome increasing?

13 July 2018

1 reference

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The role of neuronal complexes in human X-linked brain diseases

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Genomic environment predicts expression patterns on the human inactive X chromosome

13 July 2018

1 reference

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Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP)

13 July 2018

1 reference

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The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Long-term outcome in children of sex chromosome abnormalities

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Xp deletions associated with autism in three females

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Causes and associations of severe and persistent specific speech and language disorders in children

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level

13 July 2018

1 reference

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Psychiatric characteristics in a self-selected sample of boys with Klinefelter syndrome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Social behavior and autism traits in a sex chromosomal disorder: Klinefelter (47XXY) syndrome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Autism spectrum disorder and Klinefelter syndrome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Two boys with 47, XXY and autism

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Chromosomal abnormalities in a series of children with autistic disorder

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

Psychosocial competence of unselected young adults with sex chromosome abnormalities.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182523

26 September 2018

Identifiers

DOI

10.1136/ADC.2009.179747

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7 August 2017

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7 August 2017

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