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Methods in Molecular Biology (Clifton, N.J.)|February 23, 2018
A Fluorescent Quantitative Multiplex PCR Method to Detect Copy Number Changes in the RB1 GeneChitra KannabiranMolecular Vision|October 22, 2020
Review: Intraflagellar transport proteins in the retinaChitra KannabiranOphthalmic Genetics|August 18, 2020
The spermatogenesis-associated protein-7 (SPATA7) gene - an overviewChitra KannabiranJournal of Genetics|April 19, 2018
Therapeutic avenues for hereditary forms of retinal blindnessChitra Kannabiran, Indumathi MariappanHuman Mutation|May 10, 2006
TGFBI gene mutations in corneal dystrophiesChitra Kannabiran, Gordon K KlintworthFrontiers in Genetics|March 17, 2022
Genetics of Inherited Retinal Diseases in Understudied PopulationsChitra Kannabiran, Deepika Parameswarappa, Subhadra JalaliFrontiers in Medicine|September 6, 2021
Identification of Key Genes and Pathways in Persistent Hyperplastic Primary Vitreous of the Eye Using Bioinformatic AnalysisDerin M Thomas, Chitra Kannabiran, D BalasubramanianHuman Genetics|November 16, 2011
Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23Chitra Kannabiran, Hardeep Pal Singh, Subhadra JalaliCornea|November 13, 2019
Coexistence of Congenital Hereditary Endothelial Dystrophy and Fuchs Endothelial Corneal Dystrophy Associated With SLC4A11 Mutations in Affected FamiliesSunita Chaurasia, Muralidhar Ramappa, Mohini Annapurna, et al.Pageof 6