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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