ThalassemiaGlobinsHemoglobinsalpha-Globinsalpha-ThalassemiaHemoglobins, AbnormalHylobatesFetal HemoglobinHemoglobinopathiesbeta-ThalassemiaAllelesErythrocyte CountChromosomes, Human, Pair 16ReticulocytesGenesHemoglobin Abeta-GlobinsDNA Restriction EnzymesBase SequenceHemoglobin EMolecular Sequence DataTerminator Regions, GeneticHemoglobin A2DNAHemoglobin, SickleChelation TherapyLeukemia, Erythroblastic, AcuteHeterozygoteHemoglobin CAnemia, Sickle CellNucleic Acid HybridizationHemoglobin HErythropoiesisgamma-GlobinsIron OverloadRNA, MessengerErythrocytesLocus Control RegionTranscription, GeneticMutationalpha 1-AntitrypsinGenes, SwitchIron Chelating AgentsMultigene FamilyErythroid CellsChromosome DeletionErythroid Precursor CellsPromoter Regions, GeneticDNA, RecombinantHemoglobin JOxyhemoglobinsAmino Acid SequenceCloning, MolecularGene Expression RegulationChromosome MappingHomozygoteBlood TransfusionReceptors, Adrenergic, alphaHeminSickle Cell TraitHemoglobin A, GlycosylatedIronAnemiaHypoxia-Inducible Factor 1, alpha SubunitHemoglobinometryErythroblastsGenetic LinkageDeferoxamineTruncated HemoglobinsGenotypeErythrocytes, AbnormalPyridonesErythrocyte IndicesRestriction MappingNF-E2 Transcription Factor, p45 SubunitPhenotypeMethemoglobinPolymerase Chain ReactionNF-E2 Transcription FactorFerritinsOxygenErythroid-Specific DNA-Binding FactorsChromosomes, Artificial, Yeastalpha7 Nicotinic Acetylcholine ReceptorTranscription FactorsHemoglobin C DiseaseProtein BindingKineticsBinding SitesDeoxyribonuclease IK562 CellsPolymorphism, GeneticSicilyCarboxyhemoglobinMice, TransgenicHemeIntegrin alpha3beta1Integrin alpha4Integrin alpha6Liver