Lod ScoreGenetic LinkagePedigreeChromosome MappingGenetic MarkersGenes, DominantChromosomes, Human, Pair 2Microsatellite RepeatsChromosomes, Human, Pair 1Genes, RecessiveGenetic HeterogeneityHaplotypesConsanguinityGenome, HumanChromosomes, Human, Pair 6Chromosomes, Human, Pair 12Chromosomes, Human, Pair 16Chromosomes, Human, Pair 19Quantitative Trait LociChromosomes, Human, Pair 7PenetranceGenotypeNuclear FamilyChromosomes, Human, Pair 10Chromosomes, Human, Pair 4Family HealthChromosomes, Human, Pair 5Chromosomes, Human, Pair 20Quantitative Trait, HeritableGenetic Predisposition to DiseaseChromosomes, Human, Pair 3PhenotypeChromosomes, Human, Pair 13Chromosomes, Human, Pair 17X ChromosomeChromosomes, Human, Pair 9SyndromeModels, GeneticChromosomes, Human, Pair 11Age of OnsetChromosomes, Human, Pair 15Adult ChildrenCataractChromosomes, Human, Pair 8Chromosomes, HumanFamilyAllelesMatched-Pair AnalysisGenetic TestingSiblingsChromosomes, Human, Pair 18DNA Mutational AnalysisChromosomes, Human, Pair 14Polymorphism, GeneticHomozygoteRecombination, GeneticLikelihood FunctionsPolymorphism, Single NucleotidePolymorphism, Restriction Fragment LengthRetinitis PigmentosaIcelandPakistanCrosses, GeneticJewsLinkage DisequilibriumGene FrequencyMultifactorial InheritanceAbnormalities, MultipleFounder EffectChromosomes, Human, Pair 22Chromosomes, MammalianGenome-Wide Association Studybeta-Crystallin B ChainGenetic Diseases, InbornReproducibility of ResultsSeverity of Illness IndexHearing Loss, SensorineuralHypotrichosisMutationFinlandHeterozygoteDNA, SatelliteHand Deformities, CongenitalNeoplastic Syndromes, HereditaryIntellectual DisabilityCharcot-Marie-Tooth DiseaseCohort StudiesSoftwareHeterozygote DetectionGenetic LociChromosomes, Human, Pair 21ArabsEye Diseases, HereditaryChromosomes, Human, XMolecular Sequence Data