Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication

por Wang, Hong‐Dan, Liu, Lin, Wu, Dong, Li, Tao, Cui, Cun‐Ying, Zhang, Lian‐Zhong, Wang, Cheng‐Zeng
Publicado 2017

Parental Genetic Variants, MTHFR 677C>T and MTRR 66A>G, Associated Differently with Fetal Congenital Heart Defect

por Guo, Qian-nan, Wang, Hong-dan, Tie, Li-zhen, Li, Tao, Xiao, Hai, Long, Jian-gang, Liao, Shi-xiu
Publicado 2017

Collagen Type I Alpha 1 Mutation Causes Osteogenesis Imperfecta from Mild to Perinatal Death in a Chinese Family

por Liu, Hong-Yan, Huang, Jia, Wu, Dong, Li, Tao, Guo, Liang-Jie, Guo, Qian-Nan, Wang, Hong-Dan, Wang, Rui-Li, Wang, Yue
Publicado 2016

Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome

por Shi, Wei-li, Liu, Zhong-zhen, Wang, Hong-dan, Wu, Dong, Zhang, Hui, Xiao, Hai, Chu, Yan, Hou, Qiao-fang, Liao, Shi-xiu
Publicado 2016

Whole exome sequencing identifies novel mutation in eight Chinese children with isolated tetralogy of Fallot

por Liu, Lin, Wang, Hong-Dan, Cui, Cun-Ying, Qin, Yun-Yun, Fan, Tai-Bing, Peng, Bang-Tian, Zhang, Lian-Zhong, Wang, Cheng-Zeng
Publicado 2017

Cloning, expression and enzyme activity delineation of two novel CANT1 mutations: the disappearance of dimerization may indicate the change of protein conformation and even functio...

por Wang, Hong-Dan, Guo, Liang-Jie, Feng, Zhan-Qi, Zhang, Da-Wei, Zhang, Meng-Ting, Gao, Yue, Chen, Chuan-Liang, Zhu, Bo-Feng
Publicado 2020

Application of array-comparative genomic hybridization in tetralogy of Fallot

por Liu, Lin, Wang, Hong-Dan, Cui, Cun-Ying, Wu, Dong, Li, Tao, Fan, Tai-Bing, Peng, Bang-Tian, Zhang, Lian-Zhong, Wang, Cheng-Zeng
Publicado 2016

Investigating the characteristics of echocardiogram, surgical treatment, chromosome and prognosis for fetal right heart enlargement: A STROBE-compliant article

por Liu, Lin, Wang, Hong-dan, Cui, Cun-ying, Yao, Hui-mei, Huang, Lei, Li, Tao, Fan, Tai-bing, Peng, Bang-tian, Zhang, Lian-zhong
Publicado 2018

Detection of fetal epigenetic biomarkers through genome-wide DNA methylation study for non-invasive prenatal diagnosis

por Wang, Hong-Dan, Liu, Lin, Zhao, Hui-Ru, Hou, Qiao-Fang, Yan, Jing-Bin, Shi, Wei-Li, Guo, Qian-Nan, Wang, Li, Liao, Shi-Xiu, Zhu, Bo-Feng
Publicado 2017

Allele Polymorphism and Haplotype Diversity of HLA-A, -B and -DRB1 Loci in Sequence-Based Typing for Chinese Uyghur Ethnic Group

por Shen, Chun-mei, Zhu, Bo-feng, Deng, Ya-jun, Ye, Shi-hui, Yan, Jiang-wei, Yang, Guang, Wang, Hong-dan, Qin, Hai-xia, Huang, Qi-zhao, Zhang, Jing-Jing
Publicado 2010

Diagnosis with Multiple Epiphyseal Dysplasia Using Whole-exome Sequencing in a Chinese Family

por Liu, Hong-Yan, Xiao, Ji-Fang, Huang, Jia, Wang, Yue, Wu, Dong, Li, Tao, Wang, Hong-Dan, Guo, Liang-Jie, Guo, Qian-Nan, Xiao, Hai, Lyu, Xue, Yu, Zheng-Hong
Publicado 2017

Genetic polymorphism analyses of 30 InDels in Chinese Xibe ethnic group and its population genetic differentiations with other groups

por Meng, Hao-Tian, Zhang, Yu-Dang, Shen, Chun-Mei, Yuan, Guo-Lian, Yang, Chun-Hua, Jin, Rui, Yan, Jiang-Wei, Wang, Hong-Dan, Liu, Wen-Juan, Jing, Hang, Zhu, Bo-Feng
Publicado 2015

Genetic Variability and Phylogenetic Analysis of Han Population from Guanzhong Region of China based on 21 non-CODIS STR Loci

por Zhang, Yu-Dang, Tang, Xiao-Li, Meng, Hao-Tian, Wang, Hong-Dan, Jin, Rui, Yang, Chun-Hua, Yan, Jiang-Wei, Yang, Guang, Liu, Wen-Juan, Shen, Chun-Mei, Zhu, Bo-Feng
Publicado 2015

Clinical and molecular cytogenetic analyses of four patients with imbalanced translocations

por Liu, Hong Yan, Huang, Jia, Li, Tao, Wu, Dong, Wang, Hong Dan, Wang, Yue, Wang, Tao, Guo, Liang Jie, Guo, Qian Nan, Huang, Fei Fei, Wang, Rui Li, Wang, Ying Tai
Publicado 2016

DNA methylation study of fetus genome through a genome-wide analysis

por Wang, Hong-Dan, Hou, Qiao-Fang, Guo, Qian-Nan, Li, Tao, Wu, Dong, Zhang, Xian-Ping, Chu, Yan, He, Miao, Xiao, Hai, Guo, Liang-Jie, Yang, Ke, Liao, Shi-Xiu, Zhu, Bo-Feng
Publicado 2014

Genetic variation and forensic efficiency of autosomal insertion/deletion polymorphisms in Chinese Bai ethnic group: phylogenetic analysis to other populations

por Yang, Chun-Hua, Yin, Cai-Yong, Shen, Chun-Mei, Guo, Yu-Xin, Dong, Qian, Yan, Jiang-Wei, Wang, Hong-Dan, Zhang, Yu-Dang, Meng, Hao-Tian, Jin, Rui, Chen, Feng, Zhu, Bo-Feng
Publicado 2017

Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation: A case report

por Li, Tao, Zhang, Zhao-jing, Ma, Xin, Lv, Xue, Xiao, Hai, Guo, Qian-nan, Liu, Hong-yan, Wang, Hong-dan, Wu, Dong, Lou, Gui-yu, Wang, Xin, Zhang, Chao-yang, Liao, Shi-xiu
Publicado 2017

Genetic structure of Tibetan populations in Gansu revealed by forensic STR loci

por Yao, Hong-Bing, Wang, Chuan-Chao, Wang, Jiang, Tao, Xiaolan, Shang, Lei, Wen, Shao-Qing, Du, Qiajun, Deng, Qiongying, Xu, Bingying, Huang, Ying, Wang, Hong-Dan, Li, Shujin, Bin Cong, Ma, Liying, Jin, Li, Krause, Johannes, Li, Hui
Publicado 2017

Parkinson‐like early autonomic dysfunction induced by vagal application of DOPAL in rats

por Sun, Jie, He, Chao, Yan, Qiu‐Xin, Wang, Hong‐Dan, Li, Ke‐Xin, Sun, Xun, Feng, Yan, Zha, Rong‐Rong, Cui, Chang‐Peng, Xiong, Xue, Gao, Shan, Wang, Xue, Yin, Rui‐Xue, Qiao, Guo‐Fen, Li, Bai‐Yan
Publicado 2021

Distributions of HLA-A and -B alleles and haplotypes in the Yi ethnic minority of Yunnan, China: relationship to other populations

por Zhu, Bo-feng, Yang, Guang, Shen, Chun-mei, Qin, Hai-xia, Liu, Shun-zhi, Deng, Ya-jun, Fan, Shuan-liang, Deng, Li-bin, Chen, Feng, Zhang, Ping, Fang, Jie, Chen, Li-ping, Wang, Hong-dan, Wang, Zhen-yuan, Lucas, Rudolf
Publicado 2010