Lod ScoreGenetic LinkagePedigreeChromosome MappingGenetic MarkersMicrosatellite RepeatsGenes, DominantChromosomes, Human, Pair 2Chromosomes, Human, Pair 1Quantitative Trait LociGenetic HeterogeneityGenes, RecessiveHaplotypesGenome, HumanGenotypeQuantitative Trait, HeritableChromosomes, Human, Pair 12Chromosomes, Human, Pair 6Nuclear FamilyLinkage DisequilibriumGenetic Predisposition to DiseaseConsanguinityChromosomes, Human, Pair 19Chromosomes, Human, Pair 7Chromosomes, Human, Pair 10Chromosomes, Human, Pair 5Chromosomes, Human, Pair 16Models, GeneticChromosomes, Human, Pair 4Family HealthPenetrancePhenotypeChromosomes, Human, Pair 3Chromosomes, Human, Pair 20SiblingsAdult ChildrenChromosomes, Human, Pair 17X ChromosomeAllelesChromosomes, Human, Pair 11Chromosomes, HumanChromosomes, Human, Pair 9Polymorphism, Single NucleotideChromosomes, Human, Pair 13SyndromeMatched-Pair AnalysisChromosomes, Human, Pair 15Age of OnsetFamilyPolymorphism, GeneticDNA Mutational AnalysisGenome-Wide Association StudyPolymorphism, Restriction Fragment LengthLikelihood FunctionsChromosomes, Human, Pair 8Genetic TestingChromosomes, Human, Pair 14Chromosomes, Human, Pair 18Recombination, GeneticCrosses, GeneticCataractGenetic Diseases, InbornHeterozygote DetectionMultifactorial InheritanceGene FrequencyHomozygoteMutationComputer SimulationMolecular Sequence DataGenetic LociRetinitis PigmentosaSoftwareChromosomes, MammalianGenetic VariationChromosomes, Human, Pair 22Base SequenceChromosomes, Human, Pair 21HeterozygoteModels, StatisticalInheritance PatternsNeoplastic Syndromes, HereditaryDNA ProbesFounder EffectEye Diseases, HereditaryPhysical Chromosome MappingAbnormalities, MultipleChromosomes, Human, XMuscular DystrophiesDNA, SatelliteMutation, MissenseStatistics, NonparametricAsian Continental Ancestry GroupIntellectual DisabilityHearing Loss, SensorineuralGenomeCohort StudiesDNAFinlandEpilepsies, MyoclonicJews