Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'. (2015)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/ejhg.2014.275
PubMed Identifier: 25537359
Publication URI: http://europepmc.org/abstract/MED/25537359
Type: Journal Article/Review
Volume: 23
Parent Publication: European journal of human genetics : EJHG
Issue: 9
ISSN: 1018-4813