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Biochemical and Biophysical Research Communications|June 10, 1998
Identification of a recurrent missense mutation in the Norrie disease gene associated with a simplex case of exudative vitreoretinopathyB S ShastryProgress in Biophysics and Molecular Biology|January 1, 1991
Xenopus transcription factor IIIA (XTFIIIA): after a decade of researchB S ShastryClinical & Experimental Ophthalmology|January 23, 2010
Persistent hyperplastic primary vitreous: congenital malformation of the eyeBarkur S ShastryNeurochemistry International|February 28, 2003
Neurodegenerative disorders of protein aggregationBarkur S ShastryAmerican Journal of Medical Genetics|October 1, 1994
Retinitis pigmentosa and related disorders: phenotypes of rhodopsin and peripherin/RDS mutationsB S ShastryArchives of Biochemistry and Biophysics|November 1, 1993
Site-specific interaction of a partially purified human lens factor(s) with conserved sequences of the human gamma crystallin geneB S ShastryDiscovery Medicine|February 5, 2013
Genetic susceptibility to primary angle closure glaucoma (PACG)Barkur S ShastryPageof 14