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liwei
Lv1
40 积分
2024-04-17 加入
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SETD2 regulates the maternal epigenome, genomic imprinting and embryonic development
5天前
已完结
BNC1 deficiency-triggered ferroptosis through the NF2-YAP pathway induces primary ovarian insufficiency
7天前
已完结
Familial primary ovarian insufficiency associated with an SYCE1 point mutation: defective meiosis elucidated in humanized mice
7天前
已关闭
A recurrent single‐exon deletion in TBCK might be under‐recognized in patients with infantile hypotonia and psychomotor delay
11天前
已完结
The Mouse Meiotic Mutation mei1 Disrupts Chromosome Synapsis with Sexually Dimorphic Consequences for Meiotic Progression
12天前
已完结
Novel MEI1 mutations cause chromosomal and DNA methylation abnormalities leading to embryonic arrest and implantation failure
12天前
已完结
Bi-allelic MEI1 variants cause meiosis arrest and non-obstructive azoospermia
12天前
已完结
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信息写错了【积分已退回】
7天前
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