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The British Journal of Ophthalmology|September 13, 2018
Clinical profile, risk factors and outcome of medical, surgical and adjunct interventions in patients withShweta Agarwal, Geetha Iyer, Bhaskar Srinivasan, et al.Journal of Human Genetics|July 11, 2014
Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophyNagasamy Soumittra, Sampath K Loganathan, Dharanija Madhavan, et al.Human Mutation|April 3, 2007
Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. OnlineVedam L Ramprasad, Neil D Ebenezer, Tin Aung, et al.Human Molecular Genetics|November 21, 2007
SLC4A11 mutations in Fuchs endothelial corneal dystrophyEranga N Vithana, Patricio E Morgan, Vedam Ramprasad, et al.Pageof 3