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/10.17863/cam.62526

Publication URI: https://www.repository.cam.ac.uk/handle/1810/315419

Type: Other