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Ophthalmic Genetics|February 7, 2024
RPE65 mutations in Leber congenital amaurosis, early-onset severe retinal dystrophy, and retinitis pigmentosa from a tertiary eye care center in IndiaDeepika C Parameswarappa, Deepak Kumar Bagga, Abhishek Upadhyaya, et al.
Molecular Vision|September 5, 2007
SLC45A2 variations in Indian oculocutaneous albinism patientsMainak Sengupta, Moumita Chaki, N Arti, et al.
Biomed Research International|September 25, 2013
Analysis of COCH and TNFA variants in East Indian primary open-angle glaucoma patientsSubhadip Chakraborty, Suddhasil Mookherjee, Abhijit Sen, et al.
Ophthalmic Genetics|September 11, 2024
BEST1 associated bestrophinopathies with angle closure and post-surgical malignant glaucomaDeepika C Parameswarappa, Jeyapoorani Balasubramnian, Srikanta Kumar Padhy, et al.
Journal of Medical Genetics|July 11, 2006
Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11Xiaodong Jiao, Afia Sultana, Prashant Garg, et al.
Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society|August 21, 2013
RB1 gene mutations in retinoblastoma and its clinical correlationMohammad Javed Ali, Vidya Latha Parsam, Santosh G Honavar, et al.
Mutation Research|July 22, 2008
Toxicogenomics of arsenic: classical ideas and recent advancesPritha Ghosh, Mayukh Banerjee, Ashok K Giri, et al.
Environmental and Molecular Mutagenesis|November 22, 2013
Mitochondrial genome variations among arsenic exposed individuals and potential correlation with apoptotic parametersSharmistha Sinha, Ashok K Giri, Rukhsana Chowdhury, et al.
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