Exploring Spatial Relationship between Restoration Suitability and Rivers for Sustainable Wetland Utilization

por Xu, Nan, Li, Haiyan, Luo, Chunyu, Zhang, Hongqiang, Qu, Yi
Publicado 2022

COVID-19 vaccination in the mass vaccination center: clinical practice and effectiveness analysis

por Fan, Jie, Zhu, Ling, Wu, Xiaohua, Luo, Chunyu, Huang, Ailong, Wang, Wei
Publicado 2023

Pregnancy outcomes of rare autosomal trisomies results in non‐invasive prenatal screening: clinical follow‐up data from a single tertiary centre

por Lin, Ying, Hu, Ping, Li, Hang, Luo, Chunyu, Liang, Dong, Xu, Zhengfeng
Publicado 2022

A novel circ_0000654/miR‐375/E2F3 ceRNA network in esophageal squamous cell carcinoma

por Luo, Chunyu, Zhao, Xiaowei, Wang, Yuan, Li, Yanqiu, Wang, Tuo, Li, Shumin
Publicado 2022

Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysis

por MA, DINGYUAN, ZHANG, JINGJING, LUO, CHUNYU, LIN, YING, JI, XIUQING, HU, PING, XU, ZHENGFENG
Publicado 2016

Analysis of microbial differences in amniotic fluid between advanced and normal age pregnant women

por Wang, Ya, Luo, Chunyu, Cheng, Yiwei, Li, Li, Liang, Dong, Hu, Ping, Xu, Zhengfeng
Publicado 2021

A De Novo heterozygous frameshift mutation identified in BCL11B causes neurodevelopmental disorder by whole exome sequencing

por Qiao, Fengchang, Wang, Chen, Luo, Chunyu, Wang, Yan, Shao, Binbin, Tan, Jianxin, Hu, Ping, Xu, Zhengfeng
Publicado 2019

Genetic analysis of a novel SUMF1 variation associated with a late infantile form of multiple sulfatase deficiency

por Zhang, Jingjing, Ma, Dingyuan, Liu, Gang, Zeng, Huasha, Wang, Yuguo, Luo, Chunyu, Hu, Ping, Xu, Zhengfeng
Publicado 2022

Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center

por Zhang, Jingjing, Ma, Dingyuan, Liu, Gang, Wang, Yuguo, Liu, An, Li, Li, Luo, Chunyu, Hu, Ping, Xu, Zhengfeng
Publicado 2019

Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular Dystrophy

por Zhou, Jing, Tan, Jianxin, Ma, Dingyuan, Zhang, Jingjing, Cheng, Jian, Luo, Chunyu, Liu, Gang, Wang, Yuguo, Xu, Zhengfeng
Publicado 2018

A novel splice site mutation in the UBE2A gene leads to aberrant mRNA splicing in a Chinese patient with X‐linked intellectual disability type Nascimento

por Ma, Dingyuan, Tan, Jianxin, Zhou, Jing, Zhang, Jingjing, Cheng, Jian, Luo, Chunyu, Liu, Gang, Wang, Yuguo, Xu, Zhengfeng
Publicado 2019

M2 macrophage-related gene signature in chronic rhinosinusitis with nasal polyps

por Zhu, Ying, Sun, Xiwen, Tan, Shaolin, Luo, Chunyu, Zhou, Jiayao, Zhang, Shiyao, Li, Zhipeng, Lin, Hai, Zhang, Weitian
Publicado 2022

Identification and characterization of a novel 43-bp deletion mutation of the ATP7B gene in a Chinese patient with Wilson’s disease: a case report

por Liu, Gang, Ma, Dingyuan, Cheng, Jian, Zhang, Jingjing, Luo, Chunyu, Sun, Yun, Hu, Ping, Wang, Yuguo, Jiang, Tao, Xu, Zhengfeng
Publicado 2018

A Novel Whole Gene Deletion of BCKDHB by Alu-Mediated Non-allelic Recombination in a Chinese Patient With Maple Syrup Urine Disease

por Liu, Gang, Ma, Dingyuan, Hu, Ping, Wang, Wen, Luo, Chunyu, Wang, Yan, Sun, Yun, Zhang, Jingjing, Jiang, Tao, Xu, Zhengfeng
Publicado 2018

Genomic Epidemiology of an Outbreak of Klebsiella pneumoniae ST471 Producing Extended-Spectrum β-Lactamases in a Neonatal Intensive Care Unit

por Wang, Yuan, Luo, Chunyu, Du, Pengcheng, Hu, Jinrui, Zhao, Xiaowei, Mo, Dianjun, Du, Xiaoli, Xu, Xin, Li, Man, Lu, Hong, Zhou, Zhiqiang, Cui, Zhigang, Zhou, Haijian
Publicado 2020

Sinonasal diffuse large B-cell lymphoma in a patient with Wiskott–Aldrich syndrome: A case report and literature review

por Sun, Xiwen, Luo, Chunyu, Tang, Ru, Mao, Song, Zhu, Ying, Fei, Chonghui, Wang, Mengyu, Tan, Shaolin, Zhang, Shiyao, Zhou, Jiayao, Lin, Hai, Li, Zhipeng, Zhang, Weitian
Publicado 2023

Analysis of Biomarkers for Congenital Heart Disease Based on Maternal Amniotic Fluid Metabolomics

por Li, Yahong, Sun, Yun, Yang, Lan, Huang, Mingtao, Zhang, Xiaojuan, Wang, Xin, Guan, Xianwei, Yang, Peiying, Wang, Yan, Meng, Lulu, Zhou, Ran, Zhou, Xiaoyan, Luo, Chunyu, Hu, Ping, Jiang, Tao, Xu, Zhengfeng
Publicado 2021

Noninvasive prenatal diagnosis of 21-Hydroxylase deficiency using target capture sequencing of maternal plasma DNA

por Ma, Dingyuan, Yuan, Yuan, Luo, Chunyu, Wang, Yaoshen, Jiang, Tao, Guo, Fengyu, Zhang, Jingjing, Chen, Chao, Sun, Yun, Cheng, Jian, Hu, Ping, Wang, Jian, Yang, Huanming, Yi, Xin, Wang, Wei, Asan, Xu, Zhengfeng
Publicado 2017