MOESM3 of A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation (2019)
Attributed to:
A Systems Approach to Understanding Methylation Programming in Oocytes and its Consequences in Development
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.6084/m9.figshare.11393820.v1
Type: Other