ThalassemiaGlobinsHemoglobinsalpha-Globinsalpha-ThalassemiaHemoglobins, AbnormalHylobatesFetal HemoglobinHemoglobinopathiesGenes, Recessivebeta-ThalassemiaChromosomes, Human, Pair 16Erythrocyte CountReticulocytesGenesHemoglobin ABase Sequencebeta-GlobinsDNA Restriction EnzymesHemoglobin EMolecular Sequence DataConsanguinityTerminator Regions, GeneticHemoglobin A2DNAPedigreeHemoglobin, SickleMutationHeterozygoteChelation TherapyHomozygoteLeukemia, Erythroblastic, AcuteHemoglobin CChromosome MappingAnemia, Sickle CellGenetic LinkageNucleic Acid HybridizationRNA, MessengerHemoglobin HErythropoiesisgamma-GlobinsErythrocytesIron OverloadTranscription, GeneticLocus Control RegionPolycystic Kidney, Autosomal RecessiveAmino Acid SequencePhenotypealpha 1-AntitrypsinGenes, SwitchIron Chelating AgentsMultigene FamilyErythroid CellsChromosome DeletionDNA Mutational AnalysisErythroid Precursor CellsSyndromeCloning, MolecularDNA, RecombinantPromoter Regions, GeneticHemoglobin JGene Expression RegulationOxyhemoglobinsBlood TransfusionIronReceptors, Adrenergic, alphaHeminSickle Cell TraitHemoglobin A, GlycosylatedAnemiaHypoxia-Inducible Factor 1, alpha SubunitHemoglobinometryErythroblastsDeferoxamineTruncated HemoglobinsPolymerase Chain ReactionMutation, MissenseRetinitis PigmentosaGenotypeErythrocytes, AbnormalChromosomes, Artificial, YeastHeterozygote DetectionPyridonesRestriction MappingErythrocyte IndicesNF-E2 Transcription Factor, p45 SubunitExonsHaplotypesAllelesMethemoglobinProtein BindingNF-E2 Transcription FactorFerritinsLod ScoreAbnormalities, MultipleMicrocephalyTranscription FactorsOxygenErythroid-Specific DNA-Binding FactorsKinetics