Chitra Kannabiran
Kallam Anji Reddy Molecular Genetics Laboratory and Ophthalmic Pathology Service
Professor Brien Holden Eye Research Centre
L. V. Prasad Eye Institute
L.V. Prasad Marg
Name/email consistency: high
- Mutations in TULP1, NR2E3, and MFRP genes in Indian families with autosomal recessive retinitis pigmentosa. Kannabiran, C., Singh, H., Sahini, N., Jalali, S., Mohan, G. Mol. Vis. (2012)
- Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23. Kannabiran, C., Singh, H.P., Jalali, S. Hum. Genet. (2012)
- Genetics of corneal endothelial dystrophies. Kannabiran, C. J. Genet. (2009)
- Genetics of eye diseases: preface. Kannabiran, C., Ray, K. J. Genet. (2009)
- TGFBI gene mutations in corneal dystrophies. Kannabiran, C., Klintworth, G.K. Hum. Mutat. (2006)
- Genotype-phenotype correlation in 2 Indian families with severe granular corneal dystrophy. Kannabiran, C., Sridhar, M.S., Chakravarthi, S.K., Vemuganti, G.K., Lakshmipathi, M. Arch. Ophthalmol. (2005)