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A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation
H Demond, Z Anvar, BN Jahromi, A Sparago, A Verma, M Davari, ...
Genome medicine 11, 1-14, 2019
强制性开放获取政策： Fondazione Telethon, Italy, UK Biotechnology and Biological Sciences …
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