Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion. (2018)

First Author: Clissold RL

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s13148-018-0530-z

PubMed Identifier: 30021660

Publication URI: http://europepmc.org/abstract/MED/30021660

Type: Journal Article/Review

Volume: 10

Parent Publication: Clinical epigenetics

Issue: 1

ISSN: 1868-7075