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Ophthalmic Genetics, ISSN 1381-6810, 11/2018, Volume 39, Issue 6, pp. 749 - 753
Background: To report a 68-year-old female with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype associated with a subretinal hemorrhage... 
Autosomal-dominant vitreoretinochoroidopathy (ADVIRC) | subretinal hemorrhage | BEST1 | OPHTHALMOLOGY | CONE DYSFUNCTION | GENETICS & HEREDITY | Index Medicus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 11/2009, Volume 85, Issue 5, pp. 581 - 592
Journal Article
Journal Article
Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 04/2017, Volume 234, Issue 4, pp. 577 - 583
Background We investigated the relationship between prominent optic disc (POD) and inherited retinal dystrophy (IRD). Patients and Methods A cross-sectional... 
mutation | inherited retinopathy | prominent optic disc | DRUSEN | NERVE-FIBER LAYER | AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY | VITELLIFORM MACULAR DYSTROPHY | COHERENCE TOMOGRAPHY | GENE | FREQUENCY | OPHTHALMOLOGY | MUTATIONS | RETINITIS-PIGMENTOSA | RETINAL-PIGMENT EPITHELIUM
Journal Article
OPHTHALMIC GENETICS, ISSN 1381-6810, 2015, Volume 36, Issue 3, pp. 193 - 212
Journal Article
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 11/2011, Volume 32, Issue 4, pp. 217 - 227
Journal Article
JOURNAL OF GENERAL PHYSIOLOGY, ISSN 0022-1295, 05/2005, Volume 127, Issue 5, pp. 577 - 589
Mutations in VMD2, encoding bestrophin (best-1), cause Best vitelliform macular dystrophy (BMD), adult-onset vitelliform macular dystrophy (AVMD), and... 
DC-ELECTRORETINOGRAM | PHYSIOLOGY | CHLORIDE CHANNELS | DARK-ADAPTED ELECTRORETINOGRAM | VMD2 GENE | BASAL MEMBRANE | VITELLIFORM MACULAR DYSTROPHY | MOUSE BESTROPHIN-2 | CYSTIC-FIBROSIS | AUTOSOMAL-DOMINANT VITREORETINOCHOROIDOPATHY | RETINAL-PIGMENT EPITHELIUM
Journal Article
OPHTHALMOLOGE, ISSN 0941-293X, 09/2004, Volume 101, Issue 9, pp. 914 - 918
Background. Familial exudative vitreoretinopathy is a hereditary, bilaterally progressive formation of a vitreoretinal membrane. It usually occurs in full-term... 
Criswick-Schepens syndrome | PLATELET-AGGREGATION | OPHTHALMOLOGY | AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY | familial exudative vitreoretinopathy | retinopathy of prematurity | tractional retinal detachment
Journal Article
Journal Article