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