Cytochromes bBase SequenceMolecular Sequence DataCytochrome b GroupFructose IntoleranceSteroid 21-HydroxylaseAtovaquoneComplement C4aApolipoproteins BAmino Acid SequenceCyclin-Dependent Kinase Inhibitor p15Fructose-Bisphosphate AldolasePolymerase Chain ReactionPromoter Regions, GeneticMutationCloning, MolecularSequence Analysis, DNAPhylogenyDNA, MitochondrialGenesMucin-5BNail-Patella SyndromeHypobetalipoproteinemiasHepatolenticular DegenerationTranscription, GeneticAllelesGenotypePolymorphism, GeneticRNA, MessengerExonsDNA PrimersCystatin BGenetic VariationGene Expression RegulationSequence Homology, Nucleic AcidRestriction MappingAdenovirus E1B ProteinsHaplotypesDNAPulmonary Surfactant-Associated Protein BPolymorphism, Single NucleotideTranscription FactorsHypoventilationIntronsComplement C4bPhenotypePolymorphism, Restriction Fragment LengthReceptor, Melatonin, MT2Adrenal Hyperplasia, CongenitalSequence AlignmentInterleukin-12 Subunit p40DNA Mutational AnalysisHomozygoteGene FrequencySpecies SpecificitySteroid HydroxylasesAminoacyltransferasesVoltage-Gated Sodium Channel beta-2 SubunitBlotting, SouthernFructose Metabolism, Inborn ErrorsChromosome MappingGenetic Predisposition to DiseaseGene ExpressionMultigene FamilyCell LineComplement Factor BGene DeletionAbetalipoproteinemiaSteatorrheaNucleic Acid HybridizationDNA-Binding ProteinsPlasmidsEvolution, MolecularProguanilDNA Restriction EnzymesPedigreeBromoviridaeAnemia, Dyserythropoietic, CongenitalComplement C4DNA, ComplementaryInterleukinsNaphthoquinonesTransfectionAdenovirus Early ProteinsLaron SyndromeCucumovirusChromosomes, Human, Pair 9HeterozygoteHaemosporidaMonoamine OxidasePoint MutationAdenoviruses, HumanSequence Homology, Amino AcidGenetic Association StudiesClostridium difficileHistonesDeoxyribonuclease EcoRICockayne Syndrome3',5'-Cyclic-AMP PhosphodiesterasesCyclic Nucleotide Phosphodiesterases, Type 3