Novel Exon 7 Deletions in TSPAN12 in a Three-Generation FEVR Family: A Case Report and Literature Review

por Jiang, Zixuan, Wang, Panfeng
Publicado 2023

catena-Poly[[[(1,10-phenanthroline-κ(2) N,N′)praseodymium(III)]-di-μ-4-hydroxy­benzoato-κ(4) O (1):O (1′)-μ-nitrato-κ(3) O,O′:O] bis­(1,10-phenanthroline)]

por Wang, Panfeng, Xu, Dingding, Wang, Xinqing
Publicado 2012

An evaluation of OPTC and EPYC as candidate genes for high myopia

por Wang, Panfeng, Li, Shiqiang, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Publicado 2009

Genotypes and phenotypes of genes associated with achromatopsia: A reference for clinical genetic testing

por Sun, Wenmin, Li, Shiqiang, Xiao, Xueshan, Wang, Panfeng, Zhang, Qingjiong
Publicado 2020

Biomechanical evaluation of a healed acetabulum with internal fixators: finite element analysis

por Duan, Pengyun, Ding, Xiaohong, Xiong, Min, Wang, Panfeng, Xu, Shipeng, Du, Wei
Publicado 2023

Non-Pharmaceutical Interventions against COVID-19 Causing a Lower Trend in Age of LHON Onset

por Zheng, Yuxi, Jia, Xiaoyun, Li, Shiqiang, Xiao, Xueshan, Zhang, Qingjiong, Wang, Panfeng
Publicado 2023

Evaluation of MFRP as a candidate gene for high hyperopia

por Wang, Panfeng, Yang, Zhikuan, Li, Shiqiang, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Publicado 2009

Sequence variations of GRM6 in patients with high myopia

por Xu, Xiaoyu, Li, Shiqiang, Xiao, Xueshan, Wang, Panfeng, Guo, Xiangming, Zhang, Qingjiong
Publicado 2009

PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1

por Wang, Juan, Li, Shiqiang, Xiao, Xueshan, Wang, Panfeng, Guo, Xiangming, Zhang, Qingjiong
Publicado 2010

Mutation spectrum of PAX6 in Chinese patients with aniridia

por Zhang, Xiaohui, Wang, Panfeng, Li, Shiqiang, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Publicado 2011

A recurrent mutation in GUCY2D associated with autosomal dominant cone dystrophy in a Chinese family

por Xiao, Xueshan, Guo, Xiangming, Jia, Xiaoyun, Li, Shiqiang, Wang, Panfeng, Zhang, Qingjiong
Publicado 2011

Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathy

por Yang, Huiqin, Li, Shiqiang, Xiao, Xueshan, Wang, Panfeng, Guo, Xiangming, Zhang, Qingjiong
Publicado 2012

Biomechanical Comparison of Different Stabilization Constructs for Unstable Posterior Wall Fractures of Acetabulum. A Cadaveric Study

por Zhang, Yuntong, Tang, Yang, Wang, Panfeng, Zhao, Xue, Xu, Shuogui, Zhang, Chuncai
Publicado 2013

Additive Manufacturing: Unlocking the Evolution of Energy Materials

por Zhakeyev, Adilet, Wang, Panfeng, Zhang, Li, Shu, Wenmiao, Wang, Huizhi, Xuan, Jin
Publicado 2017

Rapid Synthesis of Porous Graphene Microspheres through a Three-Dimensionally Printed Inkjet Nozzle for Selective Pollutant Removal from Water

por Li, Dawei, Zhang, Hao, Zhang, Li, Wang, Panfeng, Xu, Hong, Xuan, Jin
Publicado 2019

RPE65 mutation frequency and phenotypic variation according to exome sequencing in a tertiary centre for genetic eye diseases in China

por Li, Shiqiang, Xiao, Xueshan, Yi, Zhen, Sun, Wenmin, Wang, Panfeng, Zhang, Qingjiong
Publicado 2019

Dominant RP in the Middle While Recessive in Both the N- and C-Terminals Due to RP1 Truncations: Confirmation, Refinement, and Questions

por Wang, Junwen, Xiao, Xueshan, Li, Shiqiang, Wang, Panfeng, Sun, Wenmin, Zhang, Qingjiong
Publicado 2021

Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy

por Chen, Yabin, Jia, Xiaoyun, Wang, Panfeng, Xiao, Xueshan, Li, Shiqiang, Guo, Xiangming, Zhang, Qingjiong
Publicado 2013

Novel RS1 mutations associated with X-linked juvenile retinoschisis

por YI, JUNHUI, LI, SHIQIANG, JIA, XIAOYUN, XIAO, XUESHAN, WANG, PANFENG, GUO, XIANGMING, ZHANG, QINGJIONG
Publicado 2012

Association of markers at chromosome 15q14 in Chinese patients with moderate to high myopia

por Jiao, Xiaodong, Wang, Panfeng, Li, Shiqiang, Li, Anren, Guo, Xiangming, Zhang, Qingjiong, Hejtmancik, J. Fielding
Publicado 2012