HomozygoteHeterozygoteHeterozygote DetectionGenotypeAllelesPolymorphism, GeneticMutationGene FrequencyPhenotypePedigreeGenetic Predisposition to DiseaseHemochromatosisPolymorphism, Single NucleotideGenetic VariationGenes, RecessiveHaplotypesGenes, LethalThalassemiaCrosses, GeneticPolymerase Chain ReactionHyperlipoproteinemia Type IIMice, Mutant StrainsBase SequencePoint MutationCase-Control StudiesGenes, DominantDNA Mutational AnalysisAtaxia TelangiectasiaMolecular Sequence DataMutation, MissenseHemoglobins, AbnormalExonsHyperlipoproteinemia Type IPolymorphism, Restriction Fragment LengthGenetic TestingHemoglobin EGenetic LinkageAlbinismJewsModels, GeneticChromosome MappingGenetic MarkersHemoglobin A2Apolipoprotein E2Hypobetalipoproteinemiasalpha-ThalassemiaGenetics, PopulationMethylenetetrahydrofolate Reductase (NADPH2)DNAAsian Continental Ancestry GroupFetal HemoglobinLinkage DisequilibriumCatechol O-MethyltransferaseGenetic Association StudiesRisk FactorsInbreedingHemoglobinopathiesAmino Acid SubstitutionMice, KnockoutEthylnitrosoureaShrewsalpha 1-Antitrypsin DeficiencyXanthomatosisHair ColorDNA PrimersHypolipoproteinemiasCystinuriaSelection, GeneticGlobinsMicrosatellite RepeatsGene DeletionTay-Sachs DiseaseEuropean Continental Ancestry GroupMembrane ProteinsMetabolism, Inborn ErrorsLipid Metabolism, Inborn ErrorsGenesFerritinsbeta-ThalassemiaFrameshift MutationMice, Inbred C57BLHistocompatibility Antigens Class ICystic FibrosisApolipoproteins BGlucosephosphate Dehydrogenase DeficiencyGaucher DiseaseElectrophoresis, Starch GelApolipoproteins EAdenine PhosphoribosyltransferaseLecithin Acyltransferase DeficiencyConsanguinitySequence Analysis, DNACodon, NonsenseHybrid VigorDrosophila melanogasterHyperlipoproteinemia Type IIIApolipoproteins AFamilial Mediterranean FeverAmino Acid SequenceSequence Deletion