Showing 1 - 7 results of 7 for search 'Hai-Zhu Chen', query time: 0.03s Refine Results
  1. 1
    Scheduling strategy for achieving locality in cluster

    Scheduling strategy for achieving locality in cluster by Ping GUO, Li-jiang NING, Hai-zhu CHEN

    Published 2014-11-01
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  2. 2
    Scheduling strategy for achieving locality in cluster

    Scheduling strategy for achieving locality in cluster by Ping GUO, Li-jiang NING, Hai-zhu CHEN

    Published 2014-11-01
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    Article
  3. 3
    Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients

    Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients by Feng Lin, Kang Yang, Xin Lin, Ming Jin, Long Chen, Fu-ze Zheng, Liang-liang Qiu, Zhi-xian Ye, Hai-zhu Chen, Min-ting Lin, Ning Wang, Zhi-qiang Wang

    Published 2023-11-01
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  4. 4
    A “Triple Trouble” Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy

    A “Triple Trouble” Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy by Xiao-Dan Lin, Jun-Jie He, Feng Lin, Hai-Zhu Chen, Liu-Qing Xu, Wei Hu, Nai-Qing Cai, Min-Ting Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu

    Published 2018-01-01
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  5. 5
    Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency

    Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency by Hai-Zhu Chen, Ming Jin, Nai-Qing Cai, Xiao-Dan Lin, Xin-Yi Liu, Liu-Qing Xu, Min-Ting Lin, Feng Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu, Yi Cui

    Published 2019-07-01
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  6. 6
    A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2

    A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2 by Liang-Liang Qiu, Xiao-Dan Lin, Guo-Rong Xu, Li-Li Wang, Zhi-Xian Ye, Feng Lin, Hai-Zhu Chen, Min-Ting Lin, Nai-Qing Cai, Ming Jin, Liu-Qing Xu, Wei Hu, Ning Wang, Zhi-Qiang Wang, Li-Shao Guo

    Published 2021-11-01
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  7. 7
    Loss of function of CMPK2 causes mitochondria deficiency and brain calcification

    Loss of function of CMPK2 causes mitochondria deficiency and brain calcification by Miao Zhao, Hui-Zhen Su, Yi-Heng Zeng, Yuan Sun, Xin-Xin Guo, Yun-Lu Li, Chong Wang, Zhi-Yuan Zhao, Xue-Jing Huang, Kai-Jun Lin, Zi-Ling Ye, Bi-Wei Lin, Shunyan Hong, Jitan Zheng, Yao-Bin Liu, Xiang-Ping Yao, Dehao Yang, Ying-Qian Lu, Hai-Zhu Chen, Erwei Zuo, Guang Yang, Hong-Tao Wang, Chen-Wei Huang, Xiao-Hong Lin, Zhidong Cen, Lu-Lu Lai, Yan-Ke Zhang, Xi Li, Tianmin Lai, Jingjing Lin, Dan-Dan Zuo, Min-Ting Lin, Chia-Wei Liou, Qing-Xia Kong, Chuan-Zhu Yan, Zhi-Qi Xiong, Ning Wang, Wei Luo, Cui-Ping Zhao, Xuewen Cheng, Wan-Jin Chen

    Published 2022-11-01
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