Hasil Pencarian - Guozhuang Li

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  1. 1
    P234: CCN6 copy number variant and null variant in monozygous twins with progressive pseudorheumatoid dysplasia revealed by WGS and deep phenotyping

    P234: CCN6 copy number variant and null variant in monozygous twins with progressive pseudorheumatoid dysplasia revealed by WGS and deep phenotyping oleh Kexin Xu, Guozhuang Li, Jianguo Zhang, Nan Wu

    Diterbitkan 2024-01-01
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  2. 2
    Diagnosis and treatment of the Ehlers-Danlos syndromes in China: synopsis of the first guidelines

    Diagnosis and treatment of the Ehlers-Danlos syndromes in China: synopsis of the first guidelines oleh Kexin Xu, Guozhuang Li, Zhihong Wu, Terry Jianguo Zhang, Nan Wu, On behalf of the Chinese Multi-Disciplinary Working Group on the Ehlers-Danlos Syndromes

    Diterbitkan 2024-05-01
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  3. 3
    Integrating deep phenotyping with genetic analysis: a comprehensive workflow for diagnosis and management of rare bone diseases

    Integrating deep phenotyping with genetic analysis: a comprehensive workflow for diagnosis and management of rare bone diseases oleh Guozhuang Li, Kexin Xu, Xiangjie Yin, Jianle Yang, Jihao Cai, Xinyu Yang, Qing Li, Jie Wang, Zhengye Zhao, Aoran Mahesahti, Ning Zhang, Terry Jianguo Zhang, Nan Wu

    Diterbitkan 2024-10-01
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  4. 4
    Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine

    Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine oleh Sen Zhao, Hengqiang Zhao, Lina Zhao, Xi Cheng, Zhifa Zheng, Mengfan Wu, Wen Wen, Shengru Wang, Zixiang Zhou, Haibo Xie, Dengfeng Ruan, Qing Li, Xinquan Liu, Chengzhu Ou, Guozhuang Li, Zhengye Zhao, Guilin Chen, Yuchen Niu, Xiangjie Yin, Yuhong Hu, Xiaochen Zhang, Deciphering disorders Involving Scoliosis and COmorbidities (DISCO) study, Pengfei Liu, Guixing Qiu, Wanlu Liu, Chengtian Zhao, Zhihong Wu, Jianguo Zhang, Nan Wu

    Diterbitkan 2024-02-01
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