TBX1 loss-of-function mutation contributes to congenital conotruncal defects | |
Zhang, Min; Li, Fu-Xing; Liu, Xing-Yuan; Hou, Jing-Yi; Ni, Shi-Hong; Wang, Juan; Zhao, Cui-Mei; Zhang, Wei; Kong, Ye; Huang, Ri-Tai | |
刊名 | EXPERIMENTAL AND THERAPEUTIC MEDICINE
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2018 | |
卷号 | 15期号:1 |
关键词 | congenital heart defect genetics transcription factors TBX1 reporter gene assay |
ISSN号 | 1792-0981 |
URL标识 | 查看原文 |
语种 | 英语 |
内容类型 | 期刊论文 |
URI标识 | http://www.corc.org.cn/handle/1471x/3607818 |
专题 | 复旦大学上海医学院 |
推荐引用方式 GB/T 7714 | Zhang, Min,Li, Fu-Xing,Liu, Xing-Yuan,et al. TBX1 loss-of-function mutation contributes to congenital conotruncal defects[J]. EXPERIMENTAL AND THERAPEUTIC MEDICINE,2018,15(1). |
APA | Zhang, Min.,Li, Fu-Xing.,Liu, Xing-Yuan.,Hou, Jing-Yi.,Ni, Shi-Hong.,...&Yang, Yi-Qing.(2018).TBX1 loss-of-function mutation contributes to congenital conotruncal defects.EXPERIMENTAL AND THERAPEUTIC MEDICINE,15(1). |
MLA | Zhang, Min,et al."TBX1 loss-of-function mutation contributes to congenital conotruncal defects".EXPERIMENTAL AND THERAPEUTIC MEDICINE 15.1(2018). |
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