Search Results - Zhuang, Quannan

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  1. 1
    Association of copy number variation in X chromosome-linked PNPLA4 with heterotaxy and congenital heart disease

    Association of copy number variation in X chromosome-linked PNPLA4 with heterotaxy and congenital heart disease by Gao, Han, Huang, Xianghui, Chen, Weicheng, Feng, Zhiyu, Zhao, Zhengshan, Li, Ping, Tan, Chaozhong, Wang, Jinxin, Zhuang, Quannan, Gao, Yuan, Min, Shaojie, Yao, Qinyu, Qian, Maoxiang, Ma, Xiaojing, Wu, Feizhen, Yan, Weili, Sheng, Wei, Huang, Guoying

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    An X-linked PLXNB3 mutation identified in patients with congenital heart disease with neurodevelopmental disabilities

    An X-linked PLXNB3 mutation identified in patients with congenital heart disease with neurodevelopmental disabilities by Feng, Zhiyu, Chen, Xinyuan, Li, Ting, Gao, Han, Chen, Weicheng, Gao, Yuan, Yao, Qinyu, Zhuang, Quannan, Ma, Xiaojing, Sheng, Wei, Xie, Yuquan, Huang, Guoying

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    Analysis of the CHD7 gene mutations in patients of congenital heart disease with extracardiac malformations

    Analysis of the CHD7 gene mutations in patients of congenital heart disease with extracardiac malformations by Huang, Xianghui, Gao, Han, Chen, Weicheng, Feng, Zhiyu, Tan, Chaozhong, Zhuang, Quannan, Wang, Jinxin, Gao, Yuan, Min, Shaojie, Yao, Qinyu, Sun, Jingwei, Yan, Weili, Ma, Xiaojing, Wu, Feizhen, Sheng, Wei, Huang, Guoying

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