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:
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