A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation. (2019)

First Author: Demond H
Attributed to:  Epigenome patterning in oocytes and its legacies in the embryo funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s13073-019-0694-y

PubMed Identifier: 31847873

Publication URI: http://europepmc.org/abstract/MED/31847873

Type: Journal Article/Review

Volume: 11

Parent Publication: Genome medicine

Issue: 1

ISSN: 1756-994X