1q21.1 microduplication in a patient with mental impairment and congenital heart defect

por SUN, GUOWEN, TAN, ZHIPING, FAN, LIANGLIANG, WANG, JIAN, YANG, YIFENG, ZHANG, WEIZHI
Publicado 2015

Novel heterozygous mutation in COL4A4 responsible for Alport syndrome in a Chinese family

por Du, Ran, Liu, Jishi, Hu, Yiqiao, Peng, Song, Fan, Liangliang, Xiang, Rong, Huang, Hao
Publicado 2022

Case report: A de novo Non-sense SOX9 mutation (p.Q417*) located in transactivation domain is Responsible for Campomelic Dysplasia

por Qiao, Xingxing, Wu, Liping, Tang, Jianjun, Xiang, Rong, Fan, Liangliang, Huang, Hao, Chen, Yaqin
Publicado 2023

Whole-exome sequencing detected a novel AIFM1 variant in a Han-Chinese family with Cowchock syndrome

por Wang, Chenyu, Lin, Zhaojing, Yuan, ZhuangZhuang, Tang, Tieyu, Fan, Liangliang, Liu, Yihui, Wu, Xuan
Publicado 2023

Identification of Hub Genes Associated With Clear Cell Renal Cell Carcinoma by Integrated Bioinformatics Analysis

por Huang, Hao, Zhu, Ling, Huang, Chao, Dong, Yi, Fan, Liangliang, Tao, Lijian, Peng, Zhangzhe, Xiang, Rong
Publicado 2021

Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis

por Liu, Yu-Xing, Zhang, Ai-Qian, Luo, Fang-Mei, Sheng, Yue, Wang, Chen-Yu, Dong, Yi, Fan, Liangliang, Liu, Lv
Publicado 2021

Interleukin-6, tumor necrosis factor-alpha and receptor activator of nuclear factor kappa ligand are elevated in hypertrophic gastric mucosa of pachydermoperiostosis

por Huang, Hui, Wang, Yongjun, Cao, Yong, Wu, Boda, Li, Yonggui, Fan, Liangliang, Tan, Zhiping, Jiang, Yi, Tang, Jianguang, Hu, Jianzhong, Shi, Xiaoliu
Publicado 2017