Retinal DystrophiesMuscular DystrophiesRetinal DegenerationChromosomesChromosome MappingMyotonic DystrophyLeber Congenital AmaurosisMutationMuscular Dystrophy, DuchenneMutation, MissenseRetinitis PigmentosaPoint MutationPedigreeCorneal Dystrophies, HereditaryElectroretinographycis-trans-IsomerasesX ChromosomeEye ProteinsChromosome BandingMuscular Dystrophy, AnimalFundus OculiGenes, RecessiveChromosome AberrationsConsanguinityChromosomes, Human, Pair 1Sex ChromosomesDNA Mutational AnalysisFrameshift MutationChromosomes, HumanMolecular Sequence DataGenetic LinkageChromosomes, BacterialBase SequenceFuchs' Endothelial DystrophyRetinal DiseasesLaurence-Moon SyndromePhenotypeChromosomes, Human, Pair 17Chromosomes, Human, Pair 11Chromosome SegregationChromosome DeletionChromosomes, Human, Pair 7Eye Diseases, HereditaryChromosomes, Human, Pair 6ExonsGenes, DominantChromosomes, Human, Pair 9Photoreceptor Cells, VertebrateRetinaHeterozygoteChromosomes, Human, Pair 21PeripherinsChromosomes, Human, Pair 4Muscular Dystrophy, FacioscapulohumeralBlindnessChromosomes, FungalDystrophinChromosomes, PlantChromosomes, Human, Pair 2Chromosomes, Human, Pair 19Chromosomes, Human, 6-12 and XSyndromeChromosomes, Human, Pair 16Chromosomes, Human, Pair 13Chromosomes, Human, Pair 22Chromosomes, Human, Pair 10Polymerase Chain ReactionChromosomes, MammalianCodon, NonsenseHomozygoteChromosomes, Human, XChromosome PairingGenotypeChromosome DisordersAmino Acid SequenceChromosomes, Human, Pair 8Chromosomes, Human, Pair 5Bardet-Biedl SyndromeChromosomes, Human, YMicrophthalmosPigment Epithelium of EyeNight BlindnessPolymorphism, Single-Stranded ConformationalChromosomes, Artificial, BacterialChromosomes, Human, Pair 12Germ-Line MutationLod ScoreChromosomes, Human, 1-3Chromosomes, Human, Pair 15KaryotypingPhotoreceptor CellsChromosome PaintingIn Situ Hybridization, FluorescenceAllelesSequence Analysis, DNAGenetic MarkersChromosomes, Human, Pair 20Chromosomes, Human, Pair 14Alstrom SyndromeChromosomes, Human, Pair 18