A novel PCDH19 missense mutation, c.812G>A (p.Gly271Asp), identified using whole‐exome sequencing in a Chinese family with epilepsy female restricted mental retardation syndrome

by Xuechao Zhao, Yanhong Wang, Shiyue Mei, Xiangdong Kong
Published 2020-06-01

Mutation analysis of 419 family and prenatal diagnosis of 339 cases of spinal muscular atrophy in China

by Yingjie Sun, Xiangdong Kong, Zhenhua Zhao, Xuechao Zhao
Published 2020-06-01

A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing

by Ganye Zhao, Peng Dai, Shanshan Gao, Xuechao Zhao, Conghui Wang, Lina Liu, Xiangdong Kong
Published 2019-12-01

Modification of the genome topology network and its application to the comparison of group B Streptococcus genomes

by Xiao Deng, Xuechao Zhao, Yuan Liang, Liang Zhang, Jianping Jiang, Guoping Zhao, Yan Zhou
Published 2019-11-01

Genetic analysis by targeted next-generation sequencing and novel variation identification of maple syrup urine disease in Chinese Han population

by Xiaohua Fang, Xiaofan Zhu, Yin Feng, Ying Bai, Xuechao Zhao, Xiangdong Kong, Ning Liu
Published 2021-09-01

Novel mutations of COL4A3, COL4A4, and COL4A5 genes in Chinese patients with Alport Syndrome using next generation sequence technique

by Xuechao Zhao, Chen Chen, Yanfu Wei, Ganye Zhao, Lina Liu, Conghui Wang, Junjun Zhang, Xiangdong Kong
Published 2019-06-01

An Experimental Novel Study: Angelica sinensis Prevents Epidural Fibrosis in Laminectomy Rats via Downregulation of Hydroxyproline, IL-6, and TGF-β1

by Chao Zhang, Xiaohong Kong, Hengxing Zhou, Chang Liu, Xuechao Zhao, Xianhu Zhou, Yanhua Su, Hari S. Sharma, Shiqing Feng
Published 2013-01-01