Evaluation of FOXP2 as an autism susceptibility gene (Q33960148)

30 July 2017

Evaluation of FOXP2 as an autism susceptibility gene (English)

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30 July 2017

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2

Joseph Piven

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30 July 2017

Thomas H Wassink

1

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Val C Sheffield

object named as

Val C Sheffield

7

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Veronica J Vieland

3

object named as

Veronica J Vieland

1 reference

30 July 2017

Jennifer Pietila

4

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PubMed ID

12116195

30 July 2017

Rhinda J Goedken

5

1 reference

PubMed ID

12116195

30 July 2017

Susan E Folstein

6

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30 July 2017

1 July 2002

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American Journal of Medical Genetics Part A

30 July 2017

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30 July 2017

114

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30 July 2017

5

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30 July 2017

566-569

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Genetic studies of autistic disorder and chromosome 7

30 July 2017

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

Incorporating language phenotypes strengthens evidence of linkage to autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

Polyglutamine expansion neurodegenerative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

Chromosome 7q: where autism meets language disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

A forkhead-domain gene is mutated in a severe speech and language disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

Diagnosing autism: analyses of data from the Autism Diagnostic Interview.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

Beyond the Qs in the polyglutamine diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10415

21 January 2018

Identifiers

DOI

10.1002/AJMG.10415

1 reference

30 July 2017

1 reference

PubMed ID

12116195