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Ophthalmic Genetics|July 19, 2016
Matrix metalloproteinase-1 rs1799750 polymorphism and glaucoma: A meta-analysisMiao He, Wei Wang, Xiao Han, et al.Ophthalmic Genetics|July 19, 2016
Association analysis of PPARγ (p.Pro12Ala) polymorphism with type 2 diabetic retinopathy in patients from north IndiaNavdeep Kaur, Vanita VanitaOphthalmic Genetics|November 15, 1997
Ocular manifestations of autosomal recessive Alport syndromeD Colville, J Savige, M Morfis, et al.Ophthalmic Genetics|November 15, 1997
Ocular abnormalities in a patient with partial deletion of chromosome 6p. A case reportL M Walsh, S A Lynch, M P ClarkeOphthalmic Genetics|April 29, 2020
Juvenile cataract in association with tuberous sclerosis complexA L Geffrey, K R Geenen, E Abati, et al.Ophthalmic Genetics|April 14, 2020
Association between diabetic retinopathy and interleukin-related gene polymorphisms: a machine learning aided meta-analysisXiaojun Sun, Shilei GuoOphthalmic Genetics|April 14, 2020
Is it Usher syndrome? Collaborative diagnosis and molecular genetics of patients with visual impairment and hearing lossHeather A Stiff, Christina M Sloan-Heggen, Ashley Ko, et al.Ophthalmic Genetics|April 10, 2020
TUBGCP4 - associated microcephaly and chorioretinopathyMariana Matioli Da Palma, Fabiana Louise Motta, Guilherme Eiichi Da Silva Takitani, et al.Ophthalmic Genetics|January 3, 2001
Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the familyM Van Ghelue, H L Eriksen, V Ponjavic, et al.Ophthalmic Genetics|January 3, 2001
Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormaltiesD Colville, Y Y Wang, R Jamieson, et al.Pageof 185