Clinical and genetic profiles of 985 Chinese families with skeletal dysplasia

por Li, Shanshan, Lyu, Shanshan, Fu, Wenzhen, Hu, Yunqiu, Yue, Hua, Chen, Lin, Zhang, Zhenlin
Publicado 2023

Clinical and Genetic Characteristics of Hypophosphatasia in Chinese Adults

por Li, Xiang, Ren, Na, Wang, Ziyuan, Wang, Ya, Hu, Yunqiu, Hu, Weiwei, Gu, Jiemei, Hong, Wei, Zhang, Zhenlin, Wang, Chun
Publicado 2023

Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta

por Zhang, Hao, Yue, Hua, Wang, Chun, Hu, Weiwei, Gu, Jiemei, He, Jinwei, Fu, Wenzhen, Hu, Yunqiu, Li, Miao, Zhang, Zhenlin
Publicado 2017

Association between NF-κB Signal Pathway-Related Gene Polymorphisms and Response to Alendronate Treatment in Postmenopausal Chinese Women with Low Bone Mineral Density

por Shen, Xiaoyi, Tan, Sasa, Feng, Xianzhen, Fu, Wenzhen, Hu, Yunqiu, Li, Miao, Wang, Wenjie, Yuan, Hu, Liu, Li, Wang, Chun, Hua, Fei
Publicado 2022

Genetics Evaluation of Targeted Exome Sequencing in 223 Chinese Probands With Genetic Skeletal Dysplasias

por Lv, Shanshan, Zhao, Jiao, Xi, Lei, Lin, Xiaoyun, Wang, Chun, Yue, Hua, Gu, Jiemei, Hu, Weiwei, Fu, Wenzhen, Wei, Zhanying, Zhang, Hao, Hu, Yunqiu, Li, Shanshan, Zhang, Zhenlin
Publicado 2021