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A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency
Li, Lin; Wang, Binbin; Zhang, Wei; Chen, Beili; Luo, Minna; Wang, Jing; Wang, Xi; Cao, Yunxia; Kee, Kehkooi
2017
卷号32期号:1页码:248-255
关键词primary ovarian insufficiency NOBOX homozygous truncating variant GDF9 G2 M arrest
ISSN号0268-1161
DOI10.1093/humrep/dew271
URL标识查看原文
收录类别SCIE
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/6369165
专题中国医学科学院 北京协和医学院
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Li, Lin,Wang, Binbin,Zhang, Wei,et al. A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency[J],2017,32(1):248-255.
APA Li, Lin.,Wang, Binbin.,Zhang, Wei.,Chen, Beili.,Luo, Minna.,...&Kee, Kehkooi.(2017).A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency.,32(1),248-255.
MLA Li, Lin,et al."A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency".32.1(2017):248-255.
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