📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment. (2015)

First Author: Pettigrew KA

Attributed to: Investigation of the genetic causes of Specific Language Impairment (SLI) in an isolated Chilean population funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1371/journal.pone.0134997

PubMed Identifier: 26262844

Publication URI: http://europepmc.org/abstract/MED/26262844

Type: Journal Article/Review

Volume: 10

Parent Publication: PloS one

Issue: 8

ISSN: 1932-6203