MOESM5 of A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation
收藏Figshare2019-12-17 更新2026-04-29 收录
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https://figshare.com/articles/dataset/MOESM5_of_A_KHDC3L_mutation_resulting_in_recurrent_hydatidiform_mole_causes_genome-wide_DNA_methylation_loss_in_oocytes_and_persistent_imprinting_defects_post-fertilisation/11393829
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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
