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Ophthalmic Genetics|November 4, 2022
Melphalan toxicity following treatment of retinoblastoma identified by pattern electroretinogramAlkiviades Liasis, Manuel Paez-Escamilla, Jessi Gruszewski, et al.
Ophthalmic Genetics|April 28, 2016
Vitelliform dystrophies: Prevalence in Olmsted County, Minnesota, United StatesLauren A Dalvin, Jose S Pulido, Alan D Marmorstein
Ophthalmic Genetics|April 21, 2016
Ferritin light chain gene mutation in a large Australian family with hereditary hyperferritinemia-cataract syndromeSeyhan Yazar, Maria Franchina, Jamie E Craig, et al.
Ophthalmic Genetics|February 20, 2016
Topical carbonic anhydrase inhibitors in macular edema associated with Alström syndromePaula Larrañaga-Fragoso, Natalia Pastora, Luciano Bravo-Ljubetic, et al.
Ophthalmic Genetics|August 28, 2014
MMP9 gene polymorphism is not associated with polypoidal choroidal vasculopathy and neovascular age-related macular degeneration in a Chinese Han populationRenpan Zeng, Xiongze Zhang, Kunfang Wu, et al.
Ophthalmic Genetics|January 16, 2016
Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1Simone Kellner, Heidi Stöhr, Britta Fiebig, et al.
Ophthalmic Genetics|May 18, 2016
Ocular findings in a patient with Cockayne syndrome with two mutations in the ERCC6 geneYuan Wu, Yajie Zheng, Xiaoming Yan, et al.
Ophthalmic Genetics|April 1, 2016
Putative digenic inheritance of heterozygous RP1L1 and C2orf71 null mutations in syndromic retinal dystrophyYangfan P Liu, Daniëlle G M Bosch, Anna M Siemiatkowska, et al.
Ophthalmic Genetics|February 6, 2016
Evaluation of the association of single nucleotide polymorphisms in the PRPH2 gene with adult-onset foveomacular vitelliform dystrophyMichelle Grunin, Liran Tiosano, Tareq Jaouni, et al.
Ophthalmic Genetics|February 6, 2016
Hyperferritinemia-cataract syndrome: Long-term ophthalmic observations in an Italian familyIlaria Cosentino, Fabrizio Zeri, Peter G Swann, et al.
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