HeterozygoteHeterozygote DetectionHomozygoteMutationAllelesGenotypePhenotypePedigreeDrug ResistancePolymorphism, GeneticGene FrequencyMolecular Sequence DataDrug Resistance, MicrobialBase SequenceMicrobial Sensitivity TestsThalassemiaAnti-Bacterial AgentsPolymerase Chain ReactionGenes, RecessiveGenetic VariationCrosses, GeneticHyperlipoproteinemia Type IHemoglobin A2Genes, DominantPoint MutationDNA Mutational AnalysisGenetic Predisposition to DiseaseMutation, MissenseGenes, LethalHemoglobins, AbnormalHaplotypesAtaxia TelangiectasiaHemochromatosisDrug Resistance, BacterialHyperlipoproteinemia Type IIExonsCystinuriaHypobetalipoproteinemiasTay-Sachs DiseaseMice, Mutant StrainsGenetic LinkageHemoglobin EMice, KnockoutMice, Inbred C57BLAdenine PhosphoribosyltransferaseDrug Resistance, NeoplasmChromosome MappingAmino Acid SequenceJewsModels, GeneticDNAPolymorphism, Restriction Fragment LengthSequence Analysis, DNAPolymorphism, Single NucleotideFetal HemoglobinGenetic Testingalpha-ThalassemiaGenetic MarkersDisease SusceptibilityInbreedingDrug Resistance, MultipleCell LineSelection, GeneticDNA PrimersDrug Resistance, Multiple, BacterialGenetics, PopulationHemoglobinopathiesMicrosatellite RepeatsShrewsSandhoff DiseaseGene Deletionbeta-ThalassemiaGlucosephosphate Dehydrogenase DeficiencyAmino Acid SubstitutionCells, CulturedTime FactorsRNA, MessengerFrameshift MutationAmino Acid Metabolism, Inborn ErrorsCase-Control StudiesFibroblastsGlobinsPhenylketonuriasGenesMice, Inbred StrainsPenicillin ResistanceApoptosisMembrane ProteinsCodon, NonsenseMetabolism, Inborn ErrorsCystic FibrosisLipid Metabolism, Inborn ErrorsSpecies SpecificityEscherichia coliFabry DiseaseCarrier ProteinsImmunity, InnateEthylnitrosoureaKineticsHypolipoproteinemias