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Indian Journal of Ophthalmology|August 13, 2011
Late occurrence of granular dystrophy in bilateral keratoconus: penetrating keratoplasty and long-term follow-upVarsha M Rathi, Geeta K Vemuganti, Virender S Sangwan, et al.Molecular Vision|July 4, 2008
A missense mutation in LIM2 causes autosomal recessive congenital cataractSurya Prakash G Ponnam, Kekunnaya Ramesha, Sushma Tejwani, et al.Journal of Medical Genetics|July 3, 2007
Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataractSurya Prakash G Ponnam, Kekunnaya Ramesha, Sushma Tejwani, et al.Stem Cell Research|March 13, 2024
Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3Sudipta Mahato, Savitri Maddileti, Milind Naik, et al.BMJ Case Reports|July 2, 2011
Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataractSurya Prakash G Ponnam, Kekunnaya Ramesha, Sushma Tejwani, et al.Journal of Genetics|January 22, 2010
Molecular complexity of primary open angle glaucoma: current conceptsKunal Ray, Suddhasil MookherjeeArchives of Ophthalmology (Chicago, Ill. : 1960)|August 10, 2005
Genotype-phenotype correlation in 2 Indian families with severe granular corneal dystrophyChitra Kannabiran, Mittanamalli S Sridhar, S Kalyana Chakravarthi, et al.Human Mutation|September 5, 2003
Mutational screening of the RB1 gene in Indian patients with retinoblastoma reveals eight novel and several recurrent mutationsVelamakanni Saroj Kiran, Chitra Kannabiran, Kalyana Chakravarthi, et al.Investigative Ophthalmology & Visual Science|December 30, 2004
TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patientsS V V Kalyana Chakravarthi, Chitra Kannabiran, Mittanamalli S Sridhar, et al.Journal of Genetics|January 22, 2010
A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastomaVidya Latha Parsam, Chitra Kannabiran, Santosh Honavar, et al.Pageof 14