📣 Try out the NEW Gateway to Research and let us know what you think.

We're looking for users to test the new service during August and September and share their feedback. Express your interest by completing this short form.

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

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