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SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis. 期刊论文
Genetics in medicine : official journal of the American College of Medical Genetics, 2019, 卷号: 21, 期号: 11, 页码: 2577-2585
作者:  Yang, Yongjia*;  Zheng, Yu;  Li, Wangming;  Li, Liping;  Tu, Ming
收藏  |  浏览/下载:5/0  |  提交时间:2019/12/27
BMPR1B mutation causes Pierre Robin sequence. 期刊论文
Oncotarget, 2017, 卷号: 8, 期号: 16, 页码: 25864-25871
作者:  Yang, Yongjia;  Yuan, Jianying;  Yao, Xu;  Zhang, Rong;  Yang, Hui
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/27


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