(Q48282355)

10 February 2018

title

FOXP2 in focus: what can genes tell us about speech and language? (English)

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10 February 2018

author

Simon Fisher

series ordinal

2

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10 February 2018

author name string

Gary F. Marcus

series ordinal

1

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10 February 2018

publication date

1 June 2003

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10 February 2018

Trends in Cognitive Sciences

published in

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10 February 2018

volume

7

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10 February 2018

page(s)

257-262

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10 February 2018

issue

6

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10 February 2018

Evolution at two levels in humans and chimpanzees

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The evolution of speech: a comparative review

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

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Deciphering the genetic basis of speech and language disorders

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An extended family with a dominantly inherited speech disorder

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

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

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Feature-blind grammar and dysphagia

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Speech and language defects

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

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Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia.

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Forkhead transcription factors: key players in development and metabolism

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Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors

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7 January 2021

Molecular evolution of FOXP2, a gene involved in speech and language

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Evolution and tinkering

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MRI analysis of an inherited speech and language disorder: structural brain abnormalities

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FOXP2 is not a major susceptibility gene for autism or specific language impairment

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Developmental dyslexia: genetic dissection of a complex cognitive trait

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The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo

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7 January 2021

A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye

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7 January 2021

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Identifiers

DOI

1 reference

10 February 2018

PubMed ID

12804692

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10 February 2018