Search Results - Fu Xiong

Fu Xiong

Fu Xiong, courtesy name Yuancai, originally named Pu Xiong (蒲雄), was a Di military general of Former Zhao and Former Qin during the Sixteen Kingdoms period. He was the father of Fu Jiān, the third ruler of Former Qin. During the confusion following Shi Hu's death, he served as a general under his father Pu Hong, and during the reign of his brother Fu Jiàn (note the different pinyin), he was given the role of Prime Minister. Fu Xiong's biggest contribution to the state was when he repelled a major invasion from the Grand Marshal of Jin, Huan Wen, at the Battle of Bailu Plain in 354. After Fu Jiān killed Fu Sheng and took the throne in 357, he was posthumously honoured as Emperor Wenhuan. Provided by Wikipedia
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  1. 1
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    A Novel Mutation in ATRX Causes Alpha-Thalassemia X-Linked Intellectual Disability Syndrome in a Han Chinese Family by Shaomin Wu, Shaomin Wu, Yingchun Zheng, Cailing Xu, Jiahui Fu, Fu Xiong, Fu Xiong, Fang Yang

    Published 2022
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  2. 2
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    Case Report: A Novel Compound Heterozygous Mutation of the FRMD4A Gene Identified in a Chinese Family With Global Developmental Delay, Intellectual Disability, and Ataxia by Yuhua Pan, Xiaoling Guo, Xiaoqiang Zhou, Yue Liu, Jingli Lian, Tingting Yang, Xiang Huang, Fei He, Jian Zhang, Buling Wu, Fu Xiong, Fu Xiong, Fu Xiong, Xingkun Yang

    Published 2021
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    The molecular mechanism of Gaucher disease caused by compound heterozygous mutations in GBA1 gene by Qi Liu, Zongrui Shen, Zongrui Shen, Hong Pan, Shunfei Ma, Shunfei Ma, Fu Xiong, Fu Xiong, Fei He, Fei He

    Published 2023
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    Four novel mutations identified in the COL4A3, COL4A4 and COL4A5 genes in 10 families with Alport syndrome by Duocai Wang, Meize Pan, Hang Li, Minchun Li, Ping Li, Fu Xiong, Hongbo Xiao

    Published 2024
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  5. 5
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    Functional Analysis of Ectodysplasin-A Mutations in X-Linked Nonsyndromic Hypodontia and Possible Involvement of X-Chromosome Inactivation by Yuhua Pan, Ting Lu, Ling Peng, Qi Zeng, Xiangyu Huang, Xinchen Yao, Buling Wu, Fu Xiong

    Published 2021
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    Renal-hepatic-pancreatic dysplasia-1 with a novel NPHP3 genotype: a case report and review of the literature by Hui Zhu, Zhi-hui Zhao, Shu-yao Zhu, Fu Xiong, Li-hong He, Yong Zhang, Jin Wang

    Published 2022
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    Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosis by Jianfan Chen, Xueqing Xu, Song Chen, Ting Lu, Yingchun Zheng, Zhongzhi Gan, Zongrui Shen, Shunfei Ma, Duocai Wang, Leyi Su, Fei He, Xuan Shang, Huiyong Xu, Dong Chen, Leitao Zhang, Fu Xiong

    Published 2023
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    Parental detection of neonatal jaundice using a low-cost colour card: a multicentre prospective study by Yong Zhang, Qi Jiang, Yuan Yuan, Yi Zhao, Na Chen, Yawen Li, Hui Peng, Junping Liu, Yanli Li, Jing Wei, Fu Xiong, Huimin Zhang, Yanhong Liu, Guochang Xue, Huali Zhang, Xuexing Ding, Changlin Wang, Huili Yan, Mingxing Ren, Chaoying Ma, Hanming Lu, Ruifeng Meng, Lingjun Xie, Xiufang Cheng, Jiaojiao Wang, Xiaohong Xin, Ruifen Wang, Guijuan Liang, Yuanzheng Li, Jianing Kang, Yinying Zhang, Yinglin Su, Shengjie Duan, Qingsheng Liu

    Published 2023
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