Hasil Pencarian - Xing‐Biao Qiu

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  1. 1
    PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation

    PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation oleh Xing-Biao Qiu, Ying-Jia Xu, Ruo-Gu Li, Lei Xu, Xu Liu, Wei-Yi Fang, Yi-Qing Yang, Xin-Kai Qu

    Diterbitkan 2014-01-01
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  2. 2
    A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve

    A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve oleh Wei-Feng Jiang, Ying-Jia Xu, Cui-Mei Zhao, Xin-Hua Wang, Xing-Biao Qiu, Xu Liu, Shao-Hui Wu, Yi-Qing Yang

    Diterbitkan 2020-11-01
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  3. 3
    PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.

    PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome. oleh Cui-Mei Zhao, Lu-Ying Peng, Li Li, Xing-Yuan Liu, Juan Wang, Xian-Ling Zhang, Fang Yuan, Ruo-Gu Li, Xing-Biao Qiu, Yi-Qing Yang

    Diterbitkan 2015-01-01
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  4. 4
    KLF13 Loss‐of‐Function Mutations Underlying Familial Dilated Cardiomyopathy

    KLF13 Loss‐of‐Function Mutations Underlying Familial Dilated Cardiomyopathy oleh Yu‐Han Guo, Jun Wang, Xiao‐Juan Guo, Ri‐Feng Gao, Chen‐Xi Yang, Li Li, Yu‐Min Sun, Xing‐Biao Qiu, Ying‐Jia Xu, Yi‐Qing Yang

    Diterbitkan 2022-11-01
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  5. 5
    Discovery of <i>GJC1</i> (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias

    Discovery of <i>GJC1</i> (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias oleh Yan-Jie Li, Juan Wang, Willy G. Ye, Xing-Yuan Liu, Li Li, Xing-Biao Qiu, Honghong Chen, Ying-Jia Xu, Yi-Qing Yang, Donglin Bai, Ri-Tai Huang

    Diterbitkan 2023-02-01
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  6. 6
    A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis

    A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis oleh Yu-Min Sun, Jun Wang, Xing-Biao Qiu, Fang Yuan, Ruo-Gu Li, Ying-Jia Xu, Xin-Kai Qu, Hong-Yu Shi, Xu-Min Hou, Ri-Tai Huang, Song Xue, Yi-Qing Yang

    Diterbitkan 2016-04-01
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  7. 7
    Discovery of <i>TBX20</i> as a Novel Gene Underlying Atrial Fibrillation

    Discovery of <i>TBX20</i> as a Novel Gene Underlying Atrial Fibrillation oleh Ning Li, Yan-Jie Li, Xiao-Juan Guo, Shao-Hui Wu, Wei-Feng Jiang, Dao-Liang Zhang, Kun-Wei Wang, Li Li, Yu-Min Sun, Ying-Jia Xu, Yi-Qing Yang, Xing-Biao Qiu

    Diterbitkan 2023-08-01
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  8. 8
    PRRX1 Loss‐of‐Function Mutations Underlying Familial Atrial Fibrillation

    PRRX1 Loss‐of‐Function Mutations Underlying Familial Atrial Fibrillation oleh Xiao‐Juan Guo, Xing‐Biao Qiu, Jun Wang, Yu‐Han Guo, Chen‐Xi Yang, Li Li, Ri‐Feng Gao, Zun‐Ping Ke, Ruo‐Min Di, Yu‐Min Sun, Ying‐Jia Xu, Yi‐Qing Yang

    Diterbitkan 2021-12-01
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