Lod ScoreGenetic LinkagePedigreeChromosome MappingGenetic MarkersGenes, DominantChromosomes, Human, Pair 2Microsatellite RepeatsChromosomes, Human, Pair 1Genes, RecessiveGenetic HeterogeneityHaplotypesConsanguinityGenome, HumanChromosomes, Human, Pair 6Chromosomes, Human, Pair 12Chromosomes, Human, Pair 16Quantitative Trait LociChromosomes, Human, Pair 19GenotypeChromosomes, Human, Pair 7PenetranceNuclear FamilyChromosomes, Human, Pair 10Family HealthChromosomes, Human, Pair 4Chromosomes, Human, Pair 5Genetic Predisposition to DiseaseQuantitative Trait, HeritableChromosomes, Human, Pair 20Chromosomes, Human, Pair 3PhenotypeChromosomes, Human, Pair 13Chromosomes, Human, Pair 17X ChromosomeChromosomes, Human, Pair 9SyndromeModels, GeneticAge of OnsetChromosomes, Human, Pair 11Severity of Illness IndexChromosomes, Human, Pair 15Adult ChildrenFamilyCataractChromosomes, Human, Pair 8Chromosomes, HumanAllelesMatched-Pair AnalysisGenetic TestingSiblingsReproducibility of ResultsTreatment OutcomeDNA Mutational AnalysisChromosomes, Human, Pair 18Chromosomes, Human, Pair 14Apgar ScoreQuestionnairesProspective StudiesPolymorphism, GeneticPropensity ScoreHomozygoteRecombination, GeneticLikelihood FunctionsPolymorphism, Single NucleotideCohort StudiesQuality of LifePolymorphism, Restriction Fragment LengthRetinitis PigmentosaIcelandPakistanRisk FactorsCrosses, GeneticMultifactorial InheritanceGene FrequencyLinkage DisequilibriumPredictive Value of TestsJewsFollow-Up StudiesGenome-Wide Association StudyAbnormalities, MultipleChromosomes, Human, Pair 22Founder EffectChromosomes, MammalianRetrospective StudiesSoftwareGenetic Diseases, Inbornbeta-Crystallin B ChainFinlandPain MeasurementHearing Loss, SensorineuralMutationTime FactorsHypotrichosisModels, StatisticalHeterozygoteIntellectual DisabilityDNA, SatelliteInjury Severity ScoreNeoplastic Syndromes, Hereditary