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SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis.
Yang, Yongjia*; Zheng, Yu; Li, Wangming; Li, Liping; Tu, Ming; Zhao, Liu; Mei, Haibo; Zhu, Guanghui; Zhu, Yimin*
刊名Genetics in medicine : official journal of the American College of Medical Genetics
2019
卷号21期号:11页码:2577-2585
关键词GTG banding NOG SMAD6 exome sequencing nsRUS
ISSN号1098-3600
DOI10.1038/s41436-019-0552-8
URL标识查看原文
WOS记录号WOS:000494989200022
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/5687067
专题南华大学
作者单位1.[Tu, Ming
2.Zheng, Yu
3.Zhao, Liu
4.Li, Liping
5.Yang, Yongjia
6.Zhu, Yimin
7.Yang, YJ] Univ South China, Hunan Childrens Hosp, Hunan Childrens Res Inst, Lab Genet & Metab, Changsha, Hunan, Peoples R China.
推荐引用方式
GB/T 7714
Yang, Yongjia*,Zheng, Yu,Li, Wangming,et al. SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis.[J]. Genetics in medicine : official journal of the American College of Medical Genetics,2019,21(11):2577-2585.
APA Yang, Yongjia*.,Zheng, Yu.,Li, Wangming.,Li, Liping.,Tu, Ming.,...&Zhu, Yimin*.(2019).SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis..Genetics in medicine : official journal of the American College of Medical Genetics,21(11),2577-2585.
MLA Yang, Yongjia*,et al."SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis.".Genetics in medicine : official journal of the American College of Medical Genetics 21.11(2019):2577-2585.
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