FOXP2variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum-Reference-Cited by-同舟云学术

FOXP2variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum

Published:2016-08-29 Issue:1 Volume:54 Page:64-72
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Reuter Miriam S,Riess Angelika,Moog Ute,Briggs Tracy A,Chandler Kate E,Rauch Anita,Stampfer Miriam,Steindl Katharina,Gläser Dieter,Joset Pascal,Krumbiegel Mandy,Rabe Harald,Schulte-Mattler Uta,Bauer Peter^ORCID,Beck-Wödl Stefanie,Kohlhase Jürgen,Reis André,Zweier Christiane,

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference36 articles.

1. Genetic basis of specific language impairment: evidence from a twin study;Bishop;Dev Med Child Neurol,1995

2. Genetics of spoken language disorders;Stromswold;Hum Biol,1998

3. A forkhead-domain gene is mutated in a severe speech and language disorder;Lai;Nature,2001

4. Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia;Feuk;Am J Hum Genet,2006

5. Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment;Palka;Pediatrics,2012

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