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American 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 ShastryBiochemical and Biophysical Research Communications|April 14, 1986
The use of monoclonal antibody to study the functional properties of RNA polymerase II subunitsB S ShastryExperimental Eye Research|September 1, 1989
Immunological studies on gamma crystallins from Xenopus: localization, tissue specificity and developmental expression of proteinsB S ShastryDrugs of Today (Barcelona, Spain : 1998)|January 18, 2003
Therapeutic options for Parkinson's diseaseBarkur S ShastryThe American Journal of the Medical Sciences|April 16, 1998
Molecular genetics of familial Alzheimer diseaseB S ShastryJournal of Human Genetics|February 24, 2001
Recent progress in the genetics of incontinentia pigmenti (Bloch-Sulzberger syndrome)B S ShastryMicrobial & Comparative Genomics|November 22, 2000
Mammalian cochlear genes and hereditary deafnessB S ShastryPageof 639