B. Dong

发表

Two novel PRPF31 premessenger ribonucleic acid processing factor 31 homolog mutations including a complex insertion-deletion identified in Chinese families with retinitis pigmentosa

Y. Li, Yang Li, Xiao-hui Zhang, 2013, Molecular vision.

Screening of ABCA4 Gene in a Chinese Cohort With Stargardt Disease or Cone-Rod Dystrophy With a Report on 85 Novel Mutations.

Y. Li, Yang Li, Xiao-hui Zhang, 2016, Investigative ophthalmology & visual science.

Mutation screening of mitochondrial DNA as well as OPA1 and OPA3 in a Chinese cohort with suspected hereditary optic atrophy.

Y. Li, Yang Li, Xiao-hui Zhang, 2014, Investigative Ophthalmology and Visual Science.

Novel mutations of the RS1 gene in a cohort of Chinese families with X-linked retinoschisis

Y. Li, Yang Li, Xiao-hui Zhang, 2014, Molecular vision.

Late-onset bilateral lens dislocation and glaucoma associated with a novel mutation in FBN1

Y. Li, Yang Li, Xiao-hui Zhang, 2008, Molecular vision.

A novel mutation of the VMD2 gene in a Chinese family with best vitelliform macular dystrophy.

Kang Zhang, M. Turner, B. Dong, 2006, Annals of the Academy of Medicine, Singapore.

Novel mutations in the CYP4V2 gene associated with Bietti crystalline corneoretinal dystrophy.

Y. Li, Yang Li, Yongsheng Yang, 2005, Molecular vision.

Identification of two novel OPA1 mutations in Chinese families with autosomal dominant optic atrophy

Y. Li, Yang Li, D. He, 2008, Molecular vision.

Identification of a novel ALMS1 mutation in a Chinese family with Alström syndrome

J. Li, Y. Li, L. Liu, 2009, Eye.

Two novel mutations of the PAX6 gene causing different phenotype in a cohort of Chinese patients

W. Xu, Y. Li, X. Zhang, 2011, Eye.

Identification of a novel VEGFR-3 missense mutation in a Chinese family with hereditary lymphedema type I.

Yang Li, B. Dong, Zhengya Yu, 2007, Journal of genetics and genomics = Yi chuan xue bao.

Identification of five novel mutations in the long isoform of the USH2A gene in Chinese families with Usher syndrome type II

Yang Li, Xiao-hui Zhang, B. Dong, 2008, Molecular vision.

A novel GUCY2D mutation in a Chinese family with dominant cone dystrophy

Yang Li, Xiao-hui Zhang, B. Dong, 2013, Molecular vision.

Seven novel mutations in the long isoform of the USH2A gene in Chinese families with nonsyndromic retinitis pigmentosa and Usher syndrome Type II

Yang Li, Xiao-hui Zhang, B. Dong, 2011, Molecular vision.

Comprehensive screening of CYP4V2 in a cohort of Chinese patients with Bietti crystalline dystrophy

Xiao-hui Zhang, Xiaoyan Peng, Yue Xie, 2018, Molecular vision.

Coralliform cataract caused by a novel connexin46 (GJA3) mutation in a Chinese family

Jun Wang, Yang Li, Xiao-hui Zhang, 2012, Molecular vision.

A novel connexin46 (GJA3) mutation in autosomal dominant congenital nuclear pulverulent cataract.

Jun Wang, H. Man, Yang Li, 2004, Molecular vision.

The molecular mechanisms of recombinant chromosome 18 with parental pericentric inversions and a review of the literature.

B. Dong, Lingxi Wang, Han Kang, 2023, Journal of human genetics.