Lod ScoreGenetic LinkageGenetic MarkersPedigreeChromosome MappingGenes, DominantMicrosatellite RepeatsChromosomes, Human, Pair 2Chromosomes, Human, Pair 1Genes, RecessiveBiological MarkersHaplotypesGenetic HeterogeneityConsanguinityGenome, HumanChromosomes, Human, Pair 6Chromosomes, Human, Pair 16Chromosomes, Human, Pair 12Quantitative Trait LociGenotypeChromosomes, Human, Pair 19Chromosomes, Human, Pair 7PenetranceNuclear FamilyChromosomes, Human, Pair 4Chromosomes, Human, Pair 10Family HealthChromosomes, Human, Pair 5Genetic Predisposition to DiseasePhenotypeChromosomes, Human, Pair 20Chromosomes, Human, Pair 3Quantitative Trait, HeritableChromosomes, Human, Pair 13Chromosomes, Human, Pair 17Models, GeneticX ChromosomeChromosomes, Human, Pair 9SyndromeChromosomes, Human, Pair 11AllelesAge of OnsetTumor Markers, BiologicalChromosomes, Human, Pair 15Adult ChildrenChromosomes, Human, Pair 8Chromosomes, HumanFamilyCataractGenetic TestingMatched-Pair AnalysisPolymorphism, GeneticSiblingsDNA Mutational AnalysisChromosomes, Human, Pair 18Recombination, GeneticPolymorphism, Single NucleotideChromosomes, Human, Pair 14HomozygotePolymorphism, Restriction Fragment LengthLikelihood FunctionsCrosses, GeneticLinkage DisequilibriumGene FrequencyRetinitis PigmentosaReproducibility of ResultsMutationMolecular Sequence DataIcelandPakistanGenome-Wide Association StudySeverity of Illness IndexHeterozygoteFounder EffectMultifactorial InheritanceAbnormalities, MultipleJewsChromosomes, MammalianChromosomes, Human, Pair 22Genetic LociGenetic VariationGenetic Diseases, InbornBase Sequencebeta-Crystallin B ChainDNA, SatellitePolymerase Chain ReactionHearing Loss, SensorineuralFinlandHeterozygote DetectionHypotrichosisPhysical Chromosome MappingSoftwareTreatment OutcomeIntellectual DisabilityProspective StudiesNeoplastic Syndromes, HereditaryHand Deformities, CongenitalChromosomes, Human, Pair 21Statistics, NonparametricComputer Simulation