catena-Poly[[[(1,10-phenanthroline-κ2 N,N′)praseodymium(III)]-di-μ-4-hydroxy­benzoato-κ4 O 1:O 1′-μ-nitrato-κ3 O,O′:O] bis­(1,10-phenanthroline)]

by Wang, Panfeng, Xu, Dingding, Wang, Xinqing
Published 2012

Replication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studies

by Wang, Qin, Gao, Yang, Wang, Panfeng, Li, Shiqiang, Jia, Xiaoyun, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Published 2011

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

by Xiao, Xueshan, Guo, Xiangming, Jia, Xiaoyun, Li, Shiqiang, Wang, Panfeng, Zhang, Qingjiong
Published 2011

Mutation spectrum of PAX6 in Chinese patients with aniridia

by Zhang, Xiaohui, Wang, Panfeng, Li, Shiqiang, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Published 2011

Novel RS1 mutations associated with X-linked juvenile retinoschisis

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

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

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

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

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

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

by Yang, Huiqin, Li, Shiqiang, Xiao, Xueshan, Wang, Panfeng, Guo, Xiangming, Zhang, Qingjiong
Published 2012

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

by Zhang, Yuntong, Tang, Yang, Wang, Panfeng, Zhao, Xue, Xu, Shuogui, Zhang, Chuncai
Published 2013

Degradability, biocompatibility, and osteogenesis of biocomposite scaffolds containing nano magnesium phosphate and wheat protein both in vitro and in vivo for bone regeneration

by Xia, Yan, Zhou, Panyu, Wang, Fei, Qiu, Chao, Wang, Panfeng, Zhang, Yuntong, Zhao, Liming, Xu, Shuogui
Published 2016

Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP

by Xiao, Xueshan, Li, Wei, Wang, Panfeng, Li, Lin, Li, Shiqiang, Jia, Xiaoyun, Sun, Wenmin, Guo, Xiangming, Zhang, Qingjiong
Published 2011

Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients with Leber Congenital Amaurosis

by Li, Lin, Xiao, Xueshan, Li, Shiqiang, Jia, Xiaoyun, Wang, Panfeng, Guo, Xiangming, Jiao, Xiaodong, Zhang, Qingjiong, Hejtmancik, J. Fielding
Published 2011

Evaluation of PRSS56 in Chinese subjects with high hyperopia or primary angle-closure glaucoma

by Jiang, Dan, Yang, Zhikuan, Li, Shiqiang, Xiao, Xueshan, Jia, Xiaoyun, Wang, Panfeng, Guo, Xiangming, Liu, Xing, Zhang, Qingjiong
Published 2013

Mitochondrial DNA Haplogroup Background Affects LHON, but Not Suspected LHON, in Chinese Patients

by Zhang, A-Mei, Jia, Xiaoyun, Bi, Rui, Salas, Antonio, Li, Shiqiang, Xiao, Xueshan, Wang, Panfeng, Guo, Xiangming, Kong, Qing-Peng, Zhang, Qingjiong, Yao, Yong-Gang
Published 2011

Exome Sequencing of 47 Chinese Families with Cone-Rod Dystrophy: Mutations in 25 Known Causative Genes

by Huang, Li, Zhang, Qingyan, Li, Shiqiang, Guan, Liping, Xiao, Xueshan, Zhang, Jianguo, Jia, Xiaoyun, Sun, Wenmin, Zhu, Zhihong, Gao, Yang, Yin, Ye, Wang, Panfeng, Guo, Xiangming, Wang, Jun, Zhang, Qingjiong
Published 2013