📣 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.

Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2. (2015)

First Author: Moralli D

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/10.1186/s13039-015-0148-1

PubMed Identifier: 26060509

Publication URI: http://europepmc.org/abstract/MED/26060509

Type: Journal Article/Review

Volume: 8

Parent Publication: Molecular cytogenetics

ISSN: 1755-8166