(Q50312747)

2 March 2018

title

Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31. (English)

1 reference

2 March 2018

specific language impairment

main subject

autism

0 references

1 reference

Warburton P

1

1 reference

2 March 2018

Baird G

2

1 reference

2 March 2018

Chen W

3

1 reference

2 March 2018

Morris K

4

1 reference

2 March 2018

Jacobs BW

5

1 reference

2 March 2018

Hodgson S

6

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2 March 2018

Docherty Z

7

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2 March 2018

publication date

1 April 2000

1 reference

2 March 2018

American Journal of Medical Genetics Part A

published in

1 reference

2 March 2018

volume

96

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2 March 2018

page(s)

228-234

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2 March 2018

issue

2

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2 March 2018

Genetic studies of autistic disorder and chromosome 7

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1 reference

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

21 January 2018

1 reference

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Autism: the phenotype in relatives.

21 January 2018

1 reference

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Is specific language impairment a valid diagnostic category? Genetic and psycholinguistic evidence.

21 January 2018

1 reference

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A case-control family history study of autism

21 January 2018

1 reference

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A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb.

21 January 2018

1 reference

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Localisation of a gene implicated in a severe speech and language disorder

21 January 2018

1 reference

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The epidemiology of autism: a review.

21 January 2018

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

21 January 2018

1 reference

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Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine.

21 January 2018

1 reference

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Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

21 January 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 January 2018

1 reference

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Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region

21 January 2018

1 reference

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

21 January 2018

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A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

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Familial aggregation in specific language impairment.

21 January 2018

1 reference

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Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder

21 January 2018

1 reference

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Neural basis of an inherited speech and language disorder.

21 January 2018

1 reference

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Nosological and genetic aspects of Asperger syndrome

21 January 2018

1 reference

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10.1002/(SICI)1096-8628(20000403)96:2<228::AID-AJMG20>3.0.CO;2-G

21 January 2018

Identifiers

DOI

1 reference

2 March 2018

PubMed ID

10893502

1 reference

2 March 2018