Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment-Reference-Cited by-同舟云学术

Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment

Published:2015-03-17 Issue:3 Volume:11 Page:e1004925
ISSN:1553-7404
Container-title:PLOS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Villanueva Pía,Nudel Ron,Hoischen Alexander,Fernández María Angélica,Simpson Nuala H.,Gilissen Christian,Reader Rose H.,Jara Lillian,Echeverry Maria Magdalena,Francks Clyde,Baird Gillian,Conti-Ramsden Gina,O’Hare Anne,Bolton Patrick F.,Hennessy Elizabeth R.,Palomino Hernán,Carvajal-Carmona Luis,Veltman Joris A.,Cazier Jean-Baptiste,De Barbieri Zulema,Fisher Simon E.,Newbury Dianne F.,

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics(clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference83 articles.

1. Clinical characteristics of children referred to a child development center for evaluation of speech, language, and communication disorders;S Harel;Pediatr Neurol,1996

2. Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IVTR),2000

3. Prevalence and natural history of primary speech and language delay: findings from a review of the literature;J Law;Int J Lang Commun Disord,2000

4. Is there a sex ratio difference in the familial aggregation of specific language impairment? A meta-analysis;AJ Whitehouse;J Speech Lang Hear Res,2010

5. High heritability of speech and language impairments in 6-year-old twins demonstrated using parent and teacher report;DV Bishop;Behav Genet,2006

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