MutationPoint MutationMutation, MissenseDNA Mutational AnalysisFrameshift MutationHeterozygoteFounder EffectPedigreeGenotypeJewsHomozygoteCystic Fibrosis Transmembrane Conductance RegulatorPolymerase Chain ReactionAllelesBase SequenceGenetic TestingUDPglucose-Hexose-1-Phosphate UridylyltransferaseOxidoreductases Acting on CH-NH Group DonorsMolecular Sequence DataExonsAmino Acid SubstitutionPolymorphism, Single-Stranded ConformationalCystic FibrosisGerm-Line MutationPhenotypeGene FrequencySequence DeletionBiotinidaseSteroid 21-HydroxylaseHeterozygote DetectionMethylenetetrahydrofolate Reductase (NADPH2)Keratoderma, Palmoplantar, EpidermolyticSequence Analysis, DNAKeratin-9Genes, RecessiveFamilial Mediterranean FeverHaplotypesMutation RateAmino Acid SequenceDNA PrimersGalactosemiasGaucher DiseaseDNAAdrenal Hyperplasia, CongenitalIraqCodonGene DeletionPolymorphism, GeneticDrug Resistance, ViralAsian Continental Ancestry GroupGenetic VariationFactor XI DeficiencyHyperoxaluria, PrimaryProto-Oncogene Proteins B-rafAge of OnsetCell LineMutant ProteinsGenetic Predisposition to DiseasePolymorphism, Restriction Fragment LengthMembrane ProteinsMutagenesis, Site-DirectedNeonatal ScreeningGenetic Association StudiesIntronsCodon, Nonsensebeta-ThalassemiaMutagenesisInfant, NewbornTransfectionHomocysteineCarrier ProteinsGenes, DominantMolecular Diagnostic TechniquesProtein Structure, TertiaryRifampinEscherichia coliSuppression, GeneticPolymorphism, Single NucleotideModels, MolecularChromosome MappingRNA, MessengerCricetinaeBinding SitesSequence Homology, Amino AcidDNA-Binding ProteinsGenetic Complementation TestIndiaCells, CulturedTranscription FactorsHIV-1Genes, p53SyndromeCohort StudiesCloning, MolecularProtein BindingSequence AlignmentGenetic LinkagePrevalenceCase-Control StudiesSaccharomyces cerevisiae