Retinal DystrophiesMuscular DystrophiesChromosome MappingRetinal DegenerationChromosomesMyotonic DystrophyLeber Congenital AmaurosisMuscular Dystrophy, DuchenneRetinitis PigmentosaPedigreeCorneal Dystrophies, HereditaryElectroretinographyX Chromosomecis-trans-IsomerasesChromosome BandingEye ProteinsGenetic LinkageMuscular Dystrophy, AnimalGenes, RecessiveFundus OculiConsanguinityMutationChromosomes, Human, Pair 1Chromosome AberrationsGenetic Diseases, InbornSex ChromosomesRetinal DiseasesChromosomes, HumanPhenotypeChromosomes, Human, Pair 4Fuchs' Endothelial DystrophyChromosomes, Human, Pair 17Chromosomes, Human, Pair 11Chromosomes, Human, Pair 7DNA Mutational AnalysisChromosomes, Human, Pair 6Laurence-Moon SyndromeEye Diseases, HereditaryChromosome SegregationChromosomes, BacterialChromosomes, Human, Pair 9Genetic MarkersGenes, DominantLod ScoreMolecular Sequence DataDiseaseRetinaChromosomes, Human, Pair 16Chromosome DeletionChromosomes, Human, Pair 2Photoreceptor Cells, VertebrateChromosomes, Human, Pair 21Muscular Dystrophy, FacioscapulohumeralPeripherinsChromosomes, Human, Pair 5Chromosomes, Human, Pair 19Chromosomes, Human, XChromosomes, PlantBlindnessBase SequenceChromosomes, Human, Pair 22Chromosomes, FungalChromosomes, Human, Pair 13DystrophinChromosomes, Human, 6-12 and XHaplotypesChromosomes, Human, Pair 12Chromosomes, Human, Pair 10Chromosome PairingChromosomes, MammalianSyndromeChromosome DisordersChromosomes, Human, Pair 20ExonsChromosomes, Human, YChromosomes, Human, Pair 8Pigment Epithelium of EyeBardet-Biedl SyndromeChromosomes, Artificial, YeastChromosomes, Human, 1-3Chromosomes, Artificial, BacterialMutation, MissenseChromosome PaintingChromosomes, Human, Pair 15In Situ Hybridization, FluorescenceNight BlindnessMicrophthalmosPhotoreceptor CellsHeterozygoteKaryotypingGenotypeHomozygoteExomeChromosomes, Human, Pair 14Alstrom SyndromeChromosomes, Human, Pair 18Visual AcuityDark AdaptationChromosomes, Human, 16-18Retinal Pigment Epithelium