Lod ScoreGenetic LinkagePedigreeChromosome MappingLikelihood FunctionsGenetic MarkersGenes, DominantChromosomes, Human, Pair 2Microsatellite RepeatsChromosomes, Human, Pair 1Genes, RecessiveGenetic HeterogeneityHaplotypesConsanguinityGenome, HumanChromosomes, Human, Pair 6Chromosomes, Human, Pair 12Chromosomes, Human, Pair 16Quantitative Trait LociGenotypePenetranceChromosomes, Human, Pair 19Chromosomes, Human, Pair 7Nuclear FamilyFamily HealthChromosomes, Human, Pair 10Chromosomes, Human, Pair 4Genetic Predisposition to DiseaseQuantitative Trait, HeritableChromosomes, Human, Pair 5Models, GeneticChromosomes, Human, Pair 20Chromosomes, Human, Pair 3PhenotypeChromosomes, Human, Pair 13Chromosomes, Human, Pair 17X ChromosomeChromosomes, Human, Pair 9SyndromeAge of OnsetChromosomes, Human, Pair 11Adult ChildrenFamilyChromosomes, Human, Pair 15AllelesChromosomes, HumanCataractChromosomes, Human, Pair 8Genetic TestingSiblingsMatched-Pair AnalysisDNA Mutational AnalysisChromosomes, Human, Pair 18Models, StatisticalChromosomes, Human, Pair 14Computer SimulationPolymorphism, GeneticRecombination, GeneticPolymorphism, Single NucleotideReproducibility of ResultsHomozygoteCohort StudiesGene FrequencyPolymorphism, Restriction Fragment LengthLinkage DisequilibriumSeverity of Illness IndexSoftwareRetinitis PigmentosaCrosses, GeneticIcelandRisk FactorsGenetic Diseases, InbornPakistanAlgorithmsJewsTreatment OutcomeMultifactorial InheritanceProspective StudiesFounder EffectProbabilityMutationGenome-Wide Association StudyGenetic VariationChromosomes, MammalianAbnormalities, MultipleQuestionnairesPredictive Value of TestsChromosomes, Human, Pair 22Molecular Sequence DataSensitivity and SpecificityFinlandbeta-Crystallin B ChainHeterozygoteData Interpretation, StatisticalHearing Loss, SensorineuralHypotrichosisGenetic LociHeterozygote DetectionRetrospective StudiesIntellectual Disability