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Ophthalmic Genetics|November 12, 2010
Diabetic retinopathy: Validation study of ALR2, RAGE, iNOS and TNFB gene variants in a south Indian cohortSatagopan Uthra, Rajiv Raman, Bickol N Mukesh, et al.Ophthalmic Genetics|November 12, 2010
Keratoconus associated with Williams-Beuren syndrome: first case reportsLoic Pinsard, David Touboul, Yen Vu, et al.Ophthalmic Genetics|January 28, 2011
Retinal nerve fiber thickness measurements in choroideremia patients with spectral-domain optical coherence tomographyMohamed A Genead, J Jason McAnany, Gerald A FishmanOphthalmic Genetics|December 23, 2010
Genetic linkage analyses and Cx50 mutation detection in a large multiplex Chinese family with hereditary nuclear cataractWei He, Xin Li, Jiajing Chen, et al.Ophthalmic Genetics|December 23, 2010
Juvenile xanthogranuloma of the corneoscleral limbus: report of two casesChristophe De Keyser, Prabhat Maudgal, Eric Legius, et al.Ophthalmic Genetics|December 23, 2010
A novel nonsense mutation in rhodopsin gene in two Indonesian families with autosomal recessive retinitis pigmentosaArief Kartasasmita, Keiko Fujiki, Erwin Iskandar, et al.Ophthalmic Genetics|December 23, 2010
Phenotypes in defined genotypes including siblings with Usher syndromeEva Malm, Vesna Ponjavic, Claes Möller, et al.Ophthalmic Genetics|September 3, 2010
A case report of a patient with Pfeiffer syndrome, an FGRF 2 mutation (Trp290Cys) and unique ocular anterior segment findingsGerard P Barry, Betina Mucha-Le Ny, Elaine H Zackai, et al.Ophthalmic Genetics|September 3, 2010
Historical evolution in the understanding of Stargardt macular dystrophyGerald Allen FishmanOphthalmic Genetics|September 3, 2010
Reduced frequency of known mutations in a cohort of LHON patients from IndiaPeriasamy Sundaresan, S Mahesh Kumar, Stewart Thompson, et al.Pageof 185