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Cornea, ISSN 0277-3740, 02/2015, Volume 34, Issue 2, pp. 117 - 159
PURPOSE:To update the 2008 International Classification of Corneal Dystrophies (IC3D) incorporating new clinical, histopathologic, and genetic information.... 
Fleck corneal dystrophy | Cornea | Epithelial and subepithelial dystrophies | Descemetmembrane | Posterior amorphous corneal dystrophy | Confocal microscopy | Cornea pathology | Thiel-Behnke corneal dystrophy | Lattice corneal dystrophy | Macular corneal dystrophy | Stromal dystrophies | Hereditary disease | Epithelial basement membranedystrophy | Pre-Descemet corneal dystrophy | Histopathology | Keratoconus | Congenital corneal endothelial dystrophy and X-linked endothelialdystrophy | Bowman membrane | Subepithelialmucinous corneal dystrophy | Endothelial dystrophies | Genetics | Schnyder corneal dystrophy | Gelatinousdrop-like corneal dystrophy | Fuchsendothelial corneal dystrophy | Epithelial-stromal TGFBI dystrophies | Lisch epithelial corneal dystrophy | Stroma | Histology | Meesmann dystrophy | Epithelium | Endothelium | Genetic disease | Epithelial recurrent erosion dystrophies | Posteror polymorphous corneal dystrophy | Centralcloudy dystrophy of François | Granular corneal dystrophy type 1 | Granular corneal dystrophy type 2 | TGFBI | Reis-Bücklers corneal dystrophy | Congenital stromal corneal dystrophy | Cornea dystrophy | cornea | endothelial dystrophies | histology | epithelial basement membrane dystrophy | genetic disease | epithelial and subepithelial dystrophies | central cloudy dystrophy of Francois | macular corneal dystrophy | subepithelial mucinous corneal dystrophy | cornea pathology | stroma | FRANCOIS | congenital corneal endothelial dystrophy and X-linked endothelial dystrophy | posteror polymorphous corneal dystrophy | DISEASE | epithelium | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy | pre-Descemet corneal dystrophy | histopathology | INDIVIDUAL PHENOTYPIC VARIANCES | FAMILY | epithelial recurrent erosion dystrophies | granular corneal dystrophy type 1 | granular corneal dystrophy type 2 | genetics | cornea dystrophy | UBIAD1 GENE | MUTATIONS | Descemet membrane | endothelium | hereditary disease | epithelial-stromal TGFBI dystrophies | keratoconus | posterior amorphous corneal dystrophy | congenital stromal corneal dystrophy | stromal dystrophies | fleck corneal dystrophy | confocal microscopy | gelatinous drop-like corneal dystrophy | EDEMA | OPHTHALMOLOGY | LINKAGE | Corneal Dystrophies, Hereditary - genetics | Terminology as Topic | International Classification of Diseases | Corneal Dystrophies, Hereditary - classification | Corneal Dystrophies, Hereditary - pathology | Humans | Index Medicus
Journal Article
Ophthalmology, ISSN 0161-6420, 2016, Volume 123, Issue 4, pp. 709 - 722
Journal Article
Human Mutation, ISSN 1059-7794, 04/2015, Volume 36, Issue 4, pp. 463 - 473
Journal Article
PloS one, ISSN 1932-6203, 2016, Volume 11, Issue 6, pp. e0157418 - e0157418
Purpose To report identification of a COL17A1 mutation in a family with a corneal dystrophy previously mapped to chromosome 10q23-q24. Methods Whole-exome... 
EXCLUSION | COLLAGEN | GENE | MULTIDISCIPLINARY SCIENCES | XVII | BEHNKE CORNEAL-DYSTROPHY | INDIVIDUAL PHENOTYPIC VARIANCES | CDB2 | PREDICTION | FAMILY | Autoantigens - metabolism | Epithelial Cells - metabolism | Alternative Splicing | Cytoskeletal Proteins - genetics | Humans | Corneal Dystrophies, Hereditary - genetics | Male | Epithelium, Corneal - pathology | Autoantigens - genetics | Case-Control Studies | Exome | Corneal Dystrophies, Hereditary - pathology | Genes, Dominant | Female | Gene Expression | Genome-Wide Association Study | Chromosomes, Human, Pair 10 - chemistry | Gene Frequency | Non-Fibrillar Collagens - genetics | Epithelial Cells - pathology | Chromosome Mapping | Corneal Dystrophies, Hereditary - diagnosis | Corneal Dystrophies, Hereditary - metabolism | Sequence Analysis, DNA | Non-Fibrillar Collagens - metabolism | Phenotype | Pedigree | Alleles | Epithelium, Corneal - metabolism | Heterozygote | Aged | Polymorphism, Single Nucleotide | Mutation | Cornea | Epithelial cells | Genes | Genomes | Gene sequencing | Proteins | Chromosome 10 | Genetics | Growth factors | Chromosomes | Deoxyribonucleic acid--DNA | Erosion | Phenotypes | Erosion mechanisms | Filtration | Splicing | Medicine | Gene frequency | Corneal dystrophy | Collagen | Dynamin | Dystrophy | Genetic testing | DNA sequencing | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, ISSN 0023-2165, 03/2015, Volume 232, Issue 3, pp. 283 - 294
Purpose: This report suggests how corneal dystrophies (CDs) should be diagnosed at the slit lamp and specifies the new (ICD)-D-3 classification of CDs in 2015... 
clinical diagnosis | phenotype | CLINICAL LANDMARKS | INTERNATIONAL CLASSIFICATION | ENDOTHELIAL DYSTROPHY | FRANCOIS | landmarks | International Committee for Classification of Cornea Dystrophies | (ICD)-D-3 | INDIVIDUAL PHENOTYPIC VARIANCES | IC3D CLASSIFICATION | genotype | KERATOCONUS | FAMILY | OPHTHALMOLOGY | UBIAD1 GENE | MUTATIONS
Journal Article
Environmental and Experimental Botany, ISSN 0098-8472, 09/2018, Volume 153, pp. 100 - 107
Plants respond to environmental stimuli in a diversity of ways including the production of secondary metabolites. Biosynthesis of plant phenolics, including... 
Light environment | Flavonoids | Reaction norm | Within-individual variation | Plasticity | Shade | GENOTYPE | ENVIRONMENT | ANTHOCYANINS | PLANT PIGMENTS | PLANT SCIENCES | ENVIRONMENTAL SCIENCES | EVOLUTION | BIOSYNTHESIS | DIFFERENTIATION | SELECTION | TRAITS | EXPRESSION | Anthocyanin | Gardens | Photosynthesis | Plant metabolites | Isoflavones
Journal Article
PSIKHOLOGICHESKII ZHURNAL, ISSN 0205-9592, 09/1993, Volume 14, Issue 5, pp. 67 - 72
Results of the structure analysis of the phenotype variance of cognitive activity parameters in experimental situations of different psychological structure... 
TEACHING | INDIVIDUAL DIFFERENCES | STRUCTURE OF THE PHENOTYPIC VARIANCE | COGNITIVE ACTIVITY | J VI PSYCHOLOGY
Journal Article
Wildlife Research, ISSN 1035-3712, 2013, Volume 40, Issue 7, pp. 588 - 598
Context. Long-term studies of large, vertebrate mammals using capture-recapture data are scarce, even though long-term ecological studies are requisite to... 
phenotype | repeatability | environment | white-tailed deer | individual variation | mixed model | age | SOUTH TEXAS | PHENOTYPIC PLASTICITY | BIGHORN SHEEP | RED DEER | ANTLER CHARACTERISTICS | ZOOLOGY | ECOLOGY | ANIMAL-MODEL | SOAY SHEEP | LIVE WEIGHTS | EL-NINO
Journal Article
Journal of Neurodevelopmental Disorders, ISSN 1866-1947, 12/2016, Volume 8, Issue 1, pp. 47 - 47
Background: Targeting overlapping behavioral phenotypes in neurogenetic disorders can help elucidate gene-behavior relationships. Fragile X syndrome (FXS) and... 
Longitudinal | Social behavior | Language | Fragile X syndrome | Autism spectrum disorder | Endophenotype | FMR1 gene | Pragmatics | SPECTRUM DISORDER | TRAJECTORIES | BEHAVIORAL-PHENOTYPE | MEDICINE | NEUROSCIENCES | CLINICAL NEUROLOGY | CHILDREN | INDIVIDUALS | ATTENTION-DEFICIT/HYPERACTIVITY DISORDER | BOYS | DYSFUNCTION | MALES | Autism | Development and progression | Phenotype | Genetic aspects | Research
Journal Article