MOESM5 of A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation
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Additional file 5 : Table S4. Hypomethylated regions in KHDC3Lc.1A>G mole; .xls, 56 KB
创建时间：
2019-12-17
