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Ophthalmic Genetics|September 13, 2013
Mosaic chromosome 18q partial deletion syndrome with bilateral full-thickness corneal disease: surgical intervention and histopathologyJennifer A Galvin, Russell M LeBoyer, Monica Michelotti, et al.Ophthalmic Genetics|October 12, 2013
Bilateral Concordance of the Fundus Hyperautofluorescent Ring in Typical Retinitis Pigmentosa PatientsTharikarn Sujirakul, Richard Davis, Deniz Erol, et al.Ophthalmic Genetics|October 9, 2013
Polymorphism Analysis of VSX1 and SOD1 Genes in Greek Patients with KeratoconusMarilita M Moschos, Nikolaos Kokolakis, Maria Gazouli, et al.Ophthalmic Genetics|October 9, 2013
CYP1B1 Mutations are a Major Contributor to Juvenile-Onset Open Angle Glaucoma in Saudi ArabiaKhaled K Abu-Amero, Jose Morales, Leyla A Aljasim, et al.Ophthalmic Genetics|July 10, 2013
Clinical and genetic identification of a large chinese family with autosomal dominant retinitis pigmentosaYezhen Yang, Di Tian, Janet Lee, et al.Ophthalmic Genetics|March 29, 2013
CFH (rs1410996), HTRA1 (rs112000638) and ARMS2 (rs10490923) gene polymorphisms are associated with AMD risk in Spanish patientsFernando Cruz-González, Clara Cieza-Borrella, Gloria López Valverde, et al.Ophthalmic Genetics|March 30, 2013
The role of MMP2 (-1306C>T) and TIMP2 (-418 G>C) promoter variants in age-related macular degenerationHuseyin Ortak, Selim Demir, Ömer Ateş, et al.Ophthalmic Genetics|October 2, 2013
The Role of Matrix Metalloproteinases Polymorphisms in Age-Related Macular DegenerationRasa Liutkeviciene, Vaiva Lesauskaite, Giedre Sinkunaite-Marsalkiene, et al.Ophthalmic Genetics|November 13, 2013
Analysis of catalase SNP rs1001179 in Saudi patients with primary open angle glaucomaKhaled K Abu-Amero, Altaf A Kondkar, Ahmed Mousa, et al.Ophthalmic Genetics|November 21, 2013
Retinoschisis and hyperopia associated with partial monosomy of 6q and partial trisomy of 11qNika Bagheri, Reecha S Bahl, Arun D Singh, et al.Pageof 185