Guozhuang Li (Xiaoli Chen)

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 6

Top Topics

Clinical Practice

Prognostic Factors

Ejection Fraction

Top Venues

Orphanet journal of rare diseases

Brain : a journal of neurology

The Journal of bone and joint surgery. American volume

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Kexin Xu, Guozhuang Li, Zhihong Wu, Terry Jianguo Zhang, Nan Wu, null null
Diagnosis and treatment of the Ehlers-Danlos syndromes in China: synopsis of the first guidelines. Orphanet journal of rare diseases 19 (1) (2024)
Kexin Xu, Guozhuang Li, Zhihong Wu, Terry Jianguo Zhang, Nan Wu, null null
Diagnosis and treatment of the Ehlers-Danlos syndromes in China: synopsis of the first guidelines. Orphanet journal of rare diseases 19 (1) (2024)
Kexin Xu, Guozhuang Li, Zhihong Wu, Terry Jianguo Zhang, Nan Wu, null null
Diagnosis and treatment of the Ehlers-Danlos syndromes in China: synopsis of the first guidelines. Orphanet journal of rare diseases 19 (1) (2024)
Kexin Xu, Guozhuang Li, Yuchen Niu, Zhihong Wu, null null, Terry Jianguo Zhang, Shu-Yang Zhang, Nan Wu
First copy number variant in trans with single nucleotide variant in CCN6 causing progressive pseudorheumatoid dysplasia revealed by genome sequencing and deep phenotyping in monozygotic twins. American journal of medical genetics. Part A (2024)
Nan Wu, Lian Liu, Yuanqiang Zhang, Lianlei Wang, Shengru Wang, Sen Zhao, Guozhuang Li, Yang Yang, Guanfeng Lin, Jianxiong Shen, Zhihong Wu, Guixing Qiu, Terry Jianguo Zhang
Retrospective Analysis of Associated Anomalies in 636 Patients with Operatively Treated Congenital Scoliosis. The Journal of bone and joint surgery. American volume 105 (7) (2023)
Fang Liu, Chen Liang, Zhengchang Li, Sen Zhao, Haiming Yuan, Ruen Yao, Zailong Qin, Shaofang Shangguan, Shujie Zhang, Li-Ping Zou, Qian Chen, Zhijie Gao, Suiwen Wen, Jing Peng, Fei Yin, Fei Chen, Xiaoxia Qiu, Jingsi Luo, Yingjun Xie, Dian Lu, Yu Zhang, Hua Xie, Guozhuang Li, Terry Jianguo Zhang, Pengfei Luan, Hongying Wang, Xiaodai Cui, Hailiang Huang, Ruize Liu, Xiaofang Sun, Chao Chen, Nan Wu, Jian Wang, Yanling Liu, Yiping Shen, James F Gusella, Guozhuang Li
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment. Brain : a journal of neurology (2023)