Hasil Pencarian - Terry Jianguo Zhang

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  1. 1
    Advances in clinical genetics and genomics

    Advances in clinical genetics and genomics oleh Sen Zhao, Xi Cheng, Wen Wen, Guixing Qiu, Terry Jianguo Zhang, Zhihong Wu, Nan Wu

    Diterbitkan 2021-09-01
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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
    The identification of PAX7 variants and a potential role of muscle development dysfunction in congenital scoliosis

    The identification of PAX7 variants and a potential role of muscle development dysfunction in congenital scoliosis oleh Muchuan Wang, Ziquan Li, Sen Zhao, Zhifa Zheng, Yipeng Wang, Guixing Qiu, Zhihong Wu, Nan Wu, Terry Jianguo Zhang, Siyi Cai

    Diterbitkan 2022-05-01
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  4. 4
    Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature

    Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature oleh Baoheng Gui, Baoheng Gui, Baoheng Gui, Chenxi Yu, Chenxi Yu, Xiaoxin Li, Sen Zhao, Sen Zhao, Hengqiang Zhao, Hengqiang Zhao, Zihui Yan, Zihui Yan, Xi Cheng, Xi Cheng, Jiachen Lin, Jiachen Lin, Haiyang Zheng, Haiyang Zheng, Haiyang Zheng, Jiashen Shao, Jiashen Shao, Zhengye Zhao, Zhengye Zhao, Lina Zhao, Yuchen Niu, Zhi Zhao, Huizi Wang, Bobo Xie, Bobo Xie, Bobo Xie, Xianda Wei, Xianda Wei, Chunrong Gui, Chunrong Gui, Chuan Li, Chuan Li, Chuan Li, Shaoke Chen, Shaoke Chen, Shaoke Chen, Yi Wang, Yanning Song, Chunxiu Gong, Terry Jianguo Zhang, Terry Jianguo Zhang, Terry Jianguo Zhang, Terry Jianguo Zhang

    Diterbitkan 2021-04-01
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  5. 5
    Identification of Novel FBN2 Variants in a Cohort of Congenital Contractural Arachnodactyly

    Identification of Novel FBN2 Variants in a Cohort of Congenital Contractural Arachnodactyly oleh Liying Sun, Yingzhao Huang, Yingzhao Huang, Yingzhao Huang, Sen Zhao, Sen Zhao, Sen Zhao, Wenyao Zhong, Jile Shi, Jile Shi, Jile Shi, Yang Guo, Junhui Zhao, Ge Xiong, Yuehan Yin, Zefu Chen, Zefu Chen, Zefu Chen, Nan Zhang, Zongxuan Zhao, Qingyang Li, Dan Chen, Yuchen Niu, Yuchen Niu, Xiaoxin Li, Xiaoxin Li, Guixing Qiu, Guixing Qiu, Guixing Qiu, Zhihong Wu, Zhihong Wu, Zhihong Wu, Terry Jianguo Zhang, Terry Jianguo Zhang, Terry Jianguo Zhang, Wen Tian, Nan Wu, Nan Wu, Nan Wu

    Diterbitkan 2022-03-01
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  6. 6
    Whole-genome methylation analysis reveals novel epigenetic perturbations of congenital scoliosis

    Whole-genome methylation analysis reveals novel epigenetic perturbations of congenital scoliosis oleh Gang Liu, Hengqiang Zhao, Zihui Yan, Sen Zhao, Yuchen Niu, Xiaoxin Li, Shengru Wang, Yang Yang, Sen Liu, Terry Jianguo Zhang, Zhihong Wu, Nan Wu

    Diterbitkan 2021-03-01
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  7. 7
    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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  8. 8
    Variants Affecting the C-Terminal of CSF1R Cause Congenital Vertebral Malformation Through a Gain-of-Function Mechanism

    Variants Affecting the C-Terminal of CSF1R Cause Congenital Vertebral Malformation Through a Gain-of-Function Mechanism oleh Bowen Liu, Bowen Liu, Sen Zhao, Sen Zhao, Zihui Yan, Zihui Yan, Zihui Yan, Lina Zhao, Lina Zhao, Jiachen Lin, Jiachen Lin, Jiachen Lin, Shengru Wang, Shengru Wang, Yuchen Niu, Yuchen Niu, Xiaoxin Li, Xiaoxin Li, Guixing Qiu, Guixing Qiu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Terry Jianguo Zhang, Terry Jianguo Zhang, Zhihong Wu, Zhihong Wu, Nan Wu, Nan Wu

    Diterbitkan 2021-03-01
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  9. 9
    Delineation of dual molecular diagnosis in patients with skeletal deformity

    Delineation of dual molecular diagnosis in patients with skeletal deformity oleh Lian Liu, Liying Sun, Yujun Chen, Muchuan Wang, Chenxi Yu, Yingzhao Huang, Sen Zhao, Huakang Du, Shaoke Chen, Xin Fan, Wen Tian, Zhihong Wu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study group, Guixing Qiu, Terry Jianguo Zhang, Nan Wu

    Diterbitkan 2022-03-01
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  10. 10
    The mutational burden and oligogenic inheritance in Klippel-Feil syndrome

    The mutational burden and oligogenic inheritance in Klippel-Feil syndrome oleh Ziquan Li, Sen Zhao, Siyi Cai, Yuanqiang Zhang, Lianlei Wang, Yuchen Niu, Xiaoxin Li, Jianhua Hu, Jingdan Chen, Shengru Wang, Huizi Wang, Gang Liu, Ye Tian, Zhihong Wu, Terry Jianguo Zhang, DISCO (Deciphering Disorders Involving Scoliosis and COmorbidities) study, Yipeng Wang, Nan Wu

    Diterbitkan 2020-04-01
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  11. 11
    Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis

    Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis oleh Zefu Chen, Zihui Yan, Chenxi Yu, Jiaqi Liu, Yanbin Zhang, Sen Zhao, Jiachen Lin, Yuanqiang Zhang, Lianlei Wang, Mao Lin, Yingzhao Huang, Xiaoxin Li, Yuchen Niu, Shengru Wang, Zhihong Wu, DISCO (Deciphering disorders Involving Scoliosis and COmorbidities) study group, Guixing Qiu, Terry Jianguo Zhang, Nan Wu

    Diterbitkan 2020-09-01
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  12. 12
    Deciphering the mutational signature of congenital limb malformations

    Deciphering the mutational signature of congenital limb malformations oleh Liying Sun, Yingzhao Huang, Sen Zhao, Junhui Zhao, Zihui Yan, Yang Guo, Mao Lin, Wenyao Zhong, Yuehan Yin, Zefu Chen, Nan Zhang, Yuanqiang Zhang, Zongxuan Zhao, Qingyang Li, Lianlei Wang, Xiying Dong, Yaqi Li, Xiaoxin Li, Guixing Qiu, Terry Jianguo Zhang, Zhihong Wu, Wen Tian, Nan Wu

    Diterbitkan 2021-06-01
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  13. 13
    Factors and predictive model associated with perioperative complications after long fusion in the treatment of adult non-degenerative scoliosis

    Factors and predictive model associated with perioperative complications after long fusion in the treatment of adult non-degenerative scoliosis oleh Nan Wu, Jiashen Shao, Zhen Zhang, Shengru Wang, Ziquan Li, Sen Zhao, Yang Yang, Lian Liu, Chenxi Yu, Sen Liu, Zhengye Zhao, You Du, Yuanqiang Zhang, Lianlei Wang, Yu Zhao, Keyi Yu, Hong Zhao, Jianxiong Shen, Guixing Qiu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Zhihong Wu, Terry Jianguo Zhang

    Diterbitkan 2021-05-01
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  14. 14
    Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders

    Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders oleh Sen Zhao, Yuanqiang Zhang, Sigrun Hallgrimsdottir, Yuzhi Zuo, Xiaoxin Li, Dominyka Batkovskyte, Sen Liu, Hillevi Lindelöf, Shengru Wang, Anna Hammarsjö, Yang Yang, Yongyu Ye, Lianlei Wang, Zihui Yan, Jiachen Lin, Chenxi Yu, Zefu Chen, Yuchen Niu, Huizi Wang, Zhi Zhao, Pengfei Liu, Guixing Qiu, Jennifer E. Posey, Zhihong Wu, James R. Lupski, Ieva Micule, Britt-Marie Anderlid, Ulrika Voss, Dennis Sulander, Ekaterina Kuchinskaya, Ann Nordgren, Ola Nilsson, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Terry Jianguo Zhang, Giedre Grigelioniene, Nan Wu

    Diterbitkan 2022-02-01
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  15. 15
    De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities

    De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities oleh Volkan Okur, Zefu Chen, Liesbeth Vossaert, Sandra Peacock, Jill Rosenfeld, Lina Zhao, Haowei Du, Emily Calamaro, Amanda Gerard, Sen Zhao, Jill Kelsay, Ashley Lahr, Chloe Mighton, Hillary M. Porter, Amy Siemon, Josh Silver, Shayna Svihovec, Chin-To Fong, Christina L. Grant, Jordan Lerner-Ellis, Kandamurugu Manickam, Suneeta Madan-Khetarpal, Shawn E. McCandless, Chantal F. Morel, G. Bradley Schaefer, Elizabeth M. Berry-Kravis, Ryan Gates, Natalia Gomez-Ospina, Guixing Qiu, Terry Jianguo Zhang, Zhihong Wu, Linyan Meng, Pengfei Liu, Daryl A. Scott, James R. Lupski, Christine M. Eng, Nan Wu, Bo Yuan

    Diterbitkan 2021-12-01
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