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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https://springernature.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/11393829/1
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资源简介：
Additional file 5 : Table S4. Hypomethylated regions in KHDC3Lc.1A>G mole; .xls, 56 KB
补充文件5：表S4。KHDC3L c.1A>G突变样本中的低甲基化区域；.xls格式文件，大小为56千字节。
提供机构：
figshare
创建时间：
2019-12-18
