Showing 1 - 4 results of 4 for search 'Lamei Yuan', query time: 0.01s Refine Results
  1. 1
    CADASIL: A NOTCH3-associated cerebral small vessel disease

    CADASIL: A NOTCH3-associated cerebral small vessel disease by Lamei Yuan, Xiangyu Chen, Joseph Jankovic, Hao Deng

    Published 2024-12-01
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  2. 2
    Identification of novel compound heterozygous variants in the PEX10 gene in a Han-Chinese family with PEX10-related peroxisome biogenesis disorders

    Identification of novel compound heterozygous variants in the PEX10 gene in a Han-Chinese family with PEX10-related peroxisome biogenesis disorders by Xiangjun Huang, Xinyue Deng, Xiong Deng, Hongbo Xu, Hao Deng, Lamei Yuan

    Published 2025-01-01
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  3. 3
    Correction: DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease.

    Correction: DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease. by Hong Xia, Xiangjun Huang, Sheng Deng, Hongbo Xu, Yan Yang, Xin Liu, Lamei Yuan, Hao Deng

    Published 2024-01-01
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  4. 4
    Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing.

    Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing. by Hao Deng, Qian Lu, Hongbo Xu, Xiong Deng, Lamei Yuan, Zhijian Yang, Yi Guo, Qiongfen Lin, Jingjing Xiao, Liping Guan, Zhi Song

    Published 2016-01-01
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