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Ophthalmic Genetics|March 14, 2014
Association Analysis of Polymorphisms in Genes Related to Oxidative Stress in South Indian Type 2 Diabetic Patients with RetinopathyParimala Narne, Kamakshi Chaithri Ponnaluri, Mohammed Siraj, et al.
Ophthalmic Genetics|May 20, 2008
Screening of the RPE65 gene in the Asian Indian patients with leber congenital amaurosisGandra Mamatha, Sundaramurthy Srilekha, Swaminathan Meenakshi, et al.
Ophthalmic Genetics|March 26, 2008
Association of VEGF gene polymorphisms with diabetic retinopathy in a south Indian cohortSatagopan Uthra, Rajiv Raman, Bickol N Mukesh, et al.
Ophthalmic Genetics|March 26, 2008
Novel RDH5 mutation in family with mother having fundus albipunctatus and three children with retinitis pigmentosaChunxia Wang, Nobuo Nakanishi, Kentaro Ohishi, et al.
Ophthalmic Genetics|November 17, 2018
Clinical and imaging characteristics of posterior column ataxia with retinitis pigmentosa with a specific FLVCR1 mutationJennifer Lee, Hannah L Scanga, Kunal K Dansingani, et al.
Ophthalmic Genetics|March 15, 2019
A high prevalence of biallelic RPE65 mutations in Costa Rican children with Leber congenital amaurosis and early-onset retinal dystrophyW Bailey Glen, M Millicent W Peterseim, Ramses Badilla, et al.
Ophthalmic Genetics|March 15, 2019
Protective association of A-T-T haplotype of DMT1 gene against risk of human age-related nuclear cataractRajkumar Sankaranarayanan, Nair Gopinathan Vidya, Abhay Raghukant Vasavada
Ophthalmic Genetics|April 4, 2019
Clinical and molecular findings of FRMD7 related congenital nystagmus as adifferential diagnosis of ocular albinismVincent Michaud, Sabine Defoort-Dhellemmes, Isabelle Drumare, et al.
Ophthalmic Genetics|January 28, 2017
Retinal capillaritis in a CRB1-associated retinal dystrophyVittoria Murro, Dario Pasquale Mucciolo, Andrea Sodi, et al.
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