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 8FamilyChromosomes, HumanAllelesFree RadicalsMatched-Pair AnalysisGenetic TestingSiblingsDNA Mutational AnalysisChromosomes, Human, Pair 18Chromosomes, Human, Pair 14Polymorphism, GeneticRecombination, GeneticHomozygoteLikelihood FunctionsPolymorphism, Single NucleotidePolymorphism, Restriction Fragment LengthRetinitis PigmentosaIcelandPakistanCrosses, GeneticJewsGene FrequencyLinkage DisequilibriumAbnormalities, MultipleMultifactorial InheritanceReproducibility of ResultsFounder EffectChromosomes, Human, Pair 22MutationChromosomes, MammalianGenome-Wide Association StudySeverity of Illness Indexbeta-Crystallin B ChainGenetic Diseases, InbornMolecular Sequence DataHearing Loss, SensorineuralHypotrichosisSoftwareFinlandCohort StudiesHeterozygoteComputer SimulationHand Deformities, CongenitalDNA, SatelliteIntellectual DisabilityNeoplastic Syndromes, HereditaryHeterozygote DetectionTreatment OutcomeCharcot-Marie-Tooth DiseaseGenetic LociChromosomes, Human, Pair 21ArabsEye Diseases, HereditaryChromosomes, Human, X