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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

[email]@lvpei.org

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Kallam Anji Reddy Molecular Genetics Laboratory, Hyderabad Eye Research Foundation, Hyderabad, Andhra Pradesh, India. 2005 - 2012

References

  1. 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) [Pubmed]
  2. Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23. Kannabiran, C., Singh, H.P., Jalali, S. Hum. Genet. (2012) [Pubmed]
  3. Genetics of corneal endothelial dystrophies. Kannabiran, C. J. Genet. (2009) [Pubmed]
  4. Genetics of eye diseases: preface. Kannabiran, C., Ray, K. J. Genet. (2009) [Pubmed]
  5. TGFBI gene mutations in corneal dystrophies. Kannabiran, C., Klintworth, G.K. Hum. Mutat. (2006) [Pubmed]
  6. 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) [Pubmed]
 
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