Browsing by Author Gu, Xuefan
Showing results 1 to 5 of 5
Issue Date |
Title |
Author(s) |
2019 |
Characteristics of Pompe disease in China: a report from the Pompe registry |
Zhao, Yuying;Wang, Zhaoxia;Lu, Jiahong;Gu, Xuefan;Huang, Yonglan;Qiu, Zhengqing;Wei, Yanping;Yan, Chuanzhu |
2018 |
Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions |
Fan, Yanjie;Wu, Yanming;Wang, Lili;Wang, Yu;Gong, Zhuwen;Qiu, Wenjuan;Wang, Jingmin;Zhang, Huiwen;Ji, Xing;Ye, Jun;Han, Lianshu;Jin, Xingming;Shen, Yongnian;Li, Fei;Xiao, Bing;Liang, Lili;Zhang, Xia;Liu, Xiaomin;Gu, Xuefan;Yu, Yongguo |
2010 |
Clinical, biochemical, and molecular analysis of combined methylmalonic acidemia and hyperhomocysteinemia (cblC type) in China |
Wang, Fei;Han, Lianshu;Yang, Yanling;Gu, Xuefan;Ye, Jun;Qiu, Wenjuan;Zhang, Huiwen;Zhang, Yafen;Gao, XiaoLan;Wang, Yu |
2013 |
Demographics, diagnosis and treatment of 256 patients with tetrahydrobiopterin deficiency in mainland China: results of a retrospective, multicentre study |
Ye, Jun;Yang, Yanling;Yu, Weimin;Zou, Hui;Jiang, Jianhui;Yang, Rulai;Shang, Sunny;Gu, Xuefan |
2018 |
De Novo Mutations of CCNK Cause a Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism |
Fan, Yanjie;Yin, Wu;Hu, Bing;Kline, Antonie D.;Zhang, Victor Wei;Liang, Desheng;Sun, Yu;Wang, Lili;Tang, Sha;Powis, Zoe;Li, Lei;Yan, Huifang;Shi, Zhen;Yang, Xiaoping;Chen, Yinyin;Wang, Jingmin;Jiang, Yuwu;Tan, Hu;Gu, Xuefan;Wu, Lingqian;Yu, Yongguo |