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The British Journal of Ophthalmology|May 1, 1985
A genetic linkage study of a kindred with X-linked retinitis pigmentosaS S Bhattacharya, J F Clayton, P S Harper, et al.Bioorganic & Medicinal Chemistry Letters|September 3, 2019
ω-Hydroxy isoprenoid bisphosphonates as linkable GGDPS inhibitorsNazmul H Bhuiyan, Michelle L Varney, Deep S Bhattacharya, et al.Journal of the Neurological Sciences|December 1, 1989
Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophyL V Nicholson, K Davison, M A Johnson, et al.Stem Cell Research|November 25, 2018
Generation of a human iPS cell line from a patient with retinitis pigmentosa due to EYS mutationSofia M Calado, Ana B Garcia-Delgado, Berta De la Cerda, et al.Human Reproduction (Oxford, England)|June 14, 2019
IVF for unexplained subfertility; whom should we treat?R van Eekelen, N van Geloven, M van Wely, et al.Genomics|September 1, 1991
Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment siteT J Keen, C F Inglehearn, D H Lester, et al.Annals of Human Genetics|September 7, 2007
Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRsI Barragán, S Borrego, M M Abd El-Aziz, et al.Vision Research|October 4, 2006
Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effectsAlessandro Iannaccone, David Man, Naushin Waseem, et al.Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|July 25, 2017
Optimization of beam dump shielding for K-130 cyclotron at VECCS Chatterjee, K Banerjee, Deepak Pandit, et al.Eye (London, England)|March 16, 2004
BIGH3 mutation in a Bangladeshi family with a variable phenotype of LCDIM F El-Ashry, M M Abd El-Aziz, L A Ficker, et al.Pageof 144