HeterozygoteHeterozygote DetectionHomozygoteAllelesGenotypeMutationPedigreePhenotypePolymorphism, GeneticGene FrequencyThalassemiaGenes, RecessiveHyperlipoproteinemia Type IHemoglobin A2Genetic VariationGenes, DominantDNA Mutational AnalysisGenes, LethalCrosses, GeneticBase SequenceHemoglobins, AbnormalHemochromatosisPolymerase Chain ReactionAtaxia TelangiectasiaGenetic Predisposition to DiseasePoint MutationHaplotypesHyperlipoproteinemia Type IIMutation, MissenseMolecular Sequence DataCystinuriaHypobetalipoproteinemiasTay-Sachs DiseaseExonsHemoglobin EJewsAdenine PhosphoribosyltransferaseGenetic LinkageMice, Mutant StrainsModels, GeneticFetal Hemoglobinalpha-ThalassemiaGenetic TestingPolymorphism, Single NucleotideHemoglobinopathiesChromosome MappingInbreedingGenetics, PopulationShrewsMice, KnockoutSandhoff DiseasePolymorphism, Restriction Fragment Lengthbeta-ThalassemiaGlucosephosphate Dehydrogenase DeficiencyDNAGenetic MarkersAmino Acid Metabolism, Inborn ErrorsPhenylketonuriasMicrosatellite RepeatsGlobinsFrameshift MutationSelection, GeneticLipid Metabolism, Inborn ErrorsCase-Control StudiesMetabolism, Inborn ErrorsCodon, NonsenseFabry DiseaseHypolipoproteinemiasConsanguinityHybrid VigorHexosaminidase AGene DeletionHomocystinuriaMice, Inbred C57BLLipidosesLecithin Acyltransferase DeficiencyCystic FibrosisApolipoproteins BCrossing Over, GeneticElectrophoresis, Starch GelLesch-Nyhan SyndromeDNA PrimersLipoprotein LipaseEthylnitrosoureaApolipoprotein B-100GenesSequence Analysis, DNAHaploidyalpha 1-Antitrypsin DeficiencyAlbinismChromosome InversionHemoglobin, SickleSequence Deletionbeta-N-AcetylhexosaminidasesFibroblastsHyperlipoproteinemias2-AminopurineAmino Acid SequenceLinkage DisequilibriumAsian Continental Ancestry Group