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Association of copy number variation in X chromosome-linked PNPLA4 with heterotaxy and congenital heart disease
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
Published in Chinese medical journal (05.08.2024)
Published in Chinese medical journal (05.08.2024)
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Identification of candidate genes harboring pathogenic variants in congenital heart disease and laterality defects in Chinese population
Wang, Jinxin, Chen, Weicheng, Huang, Xianghui, Gao, Han, Feng, Zhiyu, Tan, Chaozhong, Zhuang, Quannan, Gao, Yuan, Min, Shaojie, Lu, Yuquan, Wu, Feizhen, Qian, Maoxiang, Yan, Weili, Sheng, Wei, Huang, Guoying
Published in Frontiers in genetics (08.05.2025)
Published in Frontiers in genetics (08.05.2025)
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MST1R Gene Variants Predispose Individuals to Tetralogy of Fallot
Feng, Zhiyu, Huang, Xianghui, Gao, Yuan, Gao, Han, Na, Weilan, Tan, Chaozhong, Min, Shaojie, Lu, Yuquan, Zhuang, Quannan, Lin, Siyi, Ma, Xiaojing, Chen, Weicheng, Yan, Weili, Sheng, Wei, Huang, Guoying
Published in Phenomics (Cham, Switzerland) (01.12.2024)
Published in Phenomics (Cham, Switzerland) (01.12.2024)
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An X-linked PLXNB3 mutation identified in patients with congenital heart disease with neurodevelopmental disabilities
Feng, Zhiyu, Chen, Xinyuan, Li, Ting, Gao, Han, Chen, Weicheng, Gao, Yuan, Yao, Qinyu, Zhuang, Quannan, Ma, Xiaojing, Sheng, Wei, Xie, Yuquan, Huang, Guoying
Published in Translational pediatrics (01.11.2022)
Published in Translational pediatrics (01.11.2022)
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Analysis of the CHD7 gene mutations in patients of congenital heart disease with extracardiac malformations
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
Published in Translational pediatrics (30.06.2023)
Published in Translational pediatrics (30.06.2023)
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Association of copy number variation in X chromosome-linked PNPLA4 with heterotaxy and congenital heart disease
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
Published in 中华医学杂志英文版 (2024)
Published in 中华医学杂志英文版 (2024)
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