Showing results (41-50 of 59) with videos related to
Sort By:
Pageof 6
Plos One|May 19, 2017
Timing-dependent LTP and LTD in mouse primary visual cortex following different visual deprivation modelsYatu Guo, Wei Zhang, Xia Chen, et al.Molecular Vision|July 27, 2007
Two Chinese families with pulverulent congenital cataracts and deltaG91 CRYBA1 mutationsShasha Lu, Chen Zhao, Hong Jiao, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|August 30, 2012
The ophthalmology surgical competency assessment rubric for strabismus surgeryKarl C Golnik, W Walker Motley, Huban Atilla, et al.Plos One|May 17, 2014
Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2Weining Rong, Xue Chen, Kanxing Zhao, et al.Molecular Vision|April 24, 2008
Five novel mutations of the FRMD7 gene in Chinese families with X-linked infantile nystagmusNingdong Li, Liming Wang, Lihong Cui, et al.Scientific Reports|March 11, 2015
Targeted next-generation sequencing reveals novel EYS mutations in Chinese families with autosomal recessive retinitis pigmentosaXue Chen, Xiaoxing Liu, Xunlun Sheng, et al.Molecular Vision|January 16, 2014
Maternal germline mosaicism of kinesin family member 21A (KIF21A) mutation causes complex phenotypes in a Chinese family with congenital fibrosis of the extraocular musclesGang Liu, Xue Chen, Xiantao Sun, et al.Plos One|August 19, 2014
Targeted next-generation sequencing reveals novel USH2A mutations associated with diverse disease phenotypes: implications for clinical and molecular diagnosisXue Chen, Xunlun Sheng, Xiaoxing Liu, et al.Molecular Vision|December 15, 2006
An autosomal dominant progressive congenital zonular nuclear cataract linked to chromosome 20p12.2-p11.23Ningdong Li, Yongjia Yang, Juan Bu, et al.Molecular Vision|June 19, 2014
Mutation analysis of pre-mRNA splicing genes in Chinese families with retinitis pigmentosaXinyuan Pan, Xue Chen, Xiaoxing Liu, et al.Pageof 6