Lod ScoreGenetic LinkagePedigreeChromosome MappingGenetic MarkersChromosomes, Human, Pair 2Genes, DominantMicrosatellite RepeatsChromosomes, Human, Pair 1Genes, RecessiveQuantitative Trait LociGenome, HumanHaplotypesGenetic HeterogeneityConsanguinityChromosomes, Human, Pair 6Chromosomes, Human, Pair 12GenotypeChromosomes, Human, Pair 7Chromosomes, Human, Pair 16Chromosomes, Human, Pair 19Genetic Predisposition to DiseaseChromosomes, Human, Pair 10Chromosomes, Human, Pair 20Family HealthQuantitative Trait, HeritableChromosomes, Human, Pair 3Nuclear FamilyChromosomes, Human, Pair 5Chromosomes, Human, Pair 4PenetrancePhenotypeChromosomes, Human, Pair 13Chromosomes, Human, Pair 17Chromosomes, Human, Pair 11Models, GeneticSiblingsCataractChromosomes, Human, Pair 8Age of OnsetFamilyX ChromosomeChromosomes, Human, Pair 9Chromosomes, HumanSyndromeAllelesChromosomes, Human, Pair 18Genetic TestingChromosomes, Human, Pair 15Adult ChildrenDNA Mutational AnalysisPolymorphism, Single NucleotideChromosomes, MammalianCrosses, GeneticMatched-Pair AnalysisPolymorphism, GeneticVisual AcuityHomozygoteChromosomes, Human, Pair 14Likelihood FunctionsGenome-Wide Association StudyPakistanGenetic Locibeta-Crystallin A ChainReproducibility of ResultsGene FrequencyRecombination, GeneticMutationComputer SimulationPolymorphism, Restriction Fragment LengthRetinitis PigmentosaCohort StudiesEuropean Continental Ancestry GroupHeterozygoteModels, StatisticalSeverity of Illness IndexIcelandGenetic VariationAsian Continental Ancestry GroupJewsLinkage DisequilibriumTime FactorsMultifactorial InheritanceAbnormalities, MultipleMolecular Sequence DataTreatment OutcomeRegression AnalysisFounder EffectChromosomes, Human, Pair 22beta-Crystallin B ChainDiabetes Mellitus, Type 2Genetic Diseases, InbornStatistics, NonparametricHearing Loss, SensorineuralHypotrichosisRisk FactorsDNAProspective StudiesBase SequenceFinland