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Acta Ophthalmologica, ISSN 1755-375X, 09/2009, Volume 87
Journal Article
CORNEA, ISSN 0277-3740, 12/2008, Volume 27, Issue 10, pp. S1 - S42
Background: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification.... 
Grayson-Wilbrandt corneal dystrophy | Meesmann corneal dystrophy | TGFBI BIGH3 GENE | pre-Descemet corneal dystrophy | GROENOUW TYPE-I | corneal histopathology | GELSOLIN-RELATED AMYLOIDOSIS | Thiel-Behnke corneal dystrophy | posterior polymorphous corneal dystrophy | epithelial basement membrane dystrophy | POSTERIOR POLYMORPHOUS DYSTROPHY | granular corneal dystrophy 2 | COMPOUND HETEROZYGOUS MUTATIONS | granular corneal dystrophy 1 | genetic corneal disease | Schnyder corneal dystrophy | inherited corneal disease | WHORLED MICROCYSTIC DYSTROPHY | congenital hereditary endothelial dystrophy 1 | congenital hereditary endothelial dystrophy 2 | posterior amorphous corneal dystrophy | central cloudy dystrophy of Francois | macular corneal dystrophy | Schnyder crystalline corneal dystrophy | congenital stromal corneal dystrophy | gene | subepithelial mucinous corneal dystrophy | VIVO CONFOCAL MICROSCOPY | CENTRAL CLOUDY DYSTROPHY | Lisch epithelial corneal dystrophy | corneal dystrophy | eponym | X-linked endothelial corneal dystrophy | mutation | key reference | CARBOHYDRATE SULFOTRANSFERASE GENE | fleck corneal dystrophy | HEREDITARY ENDOTHELIAL DYSTROPHY | epithelial recurrent erosion dystrophy | gelatinous drop-like corneal dystrophy | OPHTHALMOLOGY | Avellino corneal dystrophy | lattice gelsolin type dystrophy | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy
Journal Article
Journal Article
Experimental Eye Research, ISSN 0014-4835, 03/2012, Volume 96, Issue 1, pp. 163 - 170
Journal Article
Journal Article
Journal Article
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 03/2009, Volume 50, Issue 3, pp. 1093 - 1097
PURPOSE. To perform a genome-wide linkage screen with a single-nucleotide polymorphism (SNP) linkage panel to identify regions of genetic linkage in Fuchs... 
CHAIN | VIII COLLAGEN | PENETRATING KERATOPLASTY | OPHTHALMOLOGY | MUTATIONS | LOCUS | COL8A2 GENE | Fuchs' Endothelial Dystrophy - genetics | Humans | Genotype | Male | Genetic Markers | Chromosomes, Human, Pair 15 - genetics | Lod Score | Pedigree | Female | Polymorphism, Single Nucleotide | Genetic Linkage - genetics | Mutation | Collagen Type VIII - genetics | Index Medicus
Journal Article
Journal Article
Cornea, ISSN 0277-3740, 10/2005, Volume 24, Issue 7, pp. 801 - 803
Journal Article
CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, ISSN 1442-6404, 11/2010, Volume 38, Issue 8, pp. 825 - 825
Journal Article
Clinical and Experimental Ophthalmology, ISSN 1442-6404, 08/2010, Volume 38, Issue 1, pp. 23 - 33
Journal Article
Clinical and Experimental Ophthalmology, ISSN 1442-6404, 2005, Volume 33, Issue 3, p. 231
The author discusses the highlights of the paper by Vincent in this issue and provides a suggestion for future research on this subject. (non-author abstract) 
Corneal Dystrophies, Hereditary, genetics | Molecular Biology | Humans | Biomedical Research | Genetic Screening
Journal Article
Journal of Molecular Biology, ISSN 0022-2836, 2011, Volume 408, Issue 3, pp. 503 - 513
Journal Article