(Q31830872)

4 July 2017

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title

Identifying autism susceptibility genes (English)

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4 July 2017

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3

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4 July 2017

Maestrini E

1

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4 July 2017

Paul A

series ordinal

2

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4 July 2017

Bailey A

series ordinal

4

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4 July 2017

language of work or name

English

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publication date

1 October 2000

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4 July 2017

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4 July 2017

volume

28

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4 July 2017

issue

1

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4 July 2017

page(s)

19-24

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Genetic studies of autistic disorder and chromosome 7

4 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Autism as a strongly genetic disorder: evidence from a British twin study

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Finding specific genes that cause autism: a combination of approaches will be needed to maximize power.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Genetic studies in autistic disorder and chromosome 15.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Evidence of linkage between the serotonin transporter and autistic disorder.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

The epidemiology of autism: a review.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Chromosomal disorders and autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Serotonin transporter (5-HTT) gene variants associated with autism?

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Imprinting mechanisms in mammals.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

A genomic screen of autism: evidence for a multilocus etiology

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Replication of linkage studies of complex traits: an examination of variation in location estimates

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

Genetics of autism: overview and new directions

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2900081-7

7 January 2021

10.1016/S0896-6273(00)00081-7

Identifiers

DOI

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4 July 2017

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