Genes, RecessiveAnemiaAnemia, HemolyticAnemia, Hemolytic, AutoimmuneConsanguinityPedigreeAnemia, Hemolytic, CongenitalHemolysisAnemia, AplasticHemolytic AgentsFanconi AnemiaMutationPolycystic Kidney, Autosomal RecessiveHomozygoteSyndromeAnemia, Hemolytic, Congenital NonspherocyticHemolytic-Uremic SyndromeDNA Mutational AnalysisAnemia, HypochromicPhenotypeGenetic LinkageAnemia, MacrocyticAnemia, PerniciousRetinitis PigmentosaMutation, MissenseAnemia, Sickle CellChromosome MappingMolecular Sequence DataHeterozygoteAbnormalities, MultipleLod ScoreMicrocephalyAnemia, MegaloblasticAnemia, SideroblasticErythrocytesHemolysin ProteinsHemoglobinsIchthyosisCoombs TestCodon, NonsenseHypotrichosisBase SequenceExonsInfectious Anemia Virus, EquineFrameshift MutationIchthyosiform Erythroderma, CongenitalAnemia, RefractoryAmino Acid SequenceHaplotypesIntellectual DisabilityGenotypeGenes, DominantAllelesPakistanAnemia, Dyserythropoietic, CongenitalFanconi Anemia Complementation Group ProteinsDeafnessIchthyosis, LamellarDwarfismHeterozygote DetectionHearing Loss, SensorineuralFounder EffectInfant, NewbornIronOsteochondrodysplasiasGenetic HeterogeneityComplement Hemolytic Activity AssayCerebellar AtaxiaPoint MutationErythropoietinMuscular DystrophiesFamily HealthHemolytic Plaque TechniqueEquine Infectious AnemiaGenetic MarkersOsteopetrosisSpherocytosis, HereditaryErythroblastosis, FetalFanconi Anemia Complementation Group A ProteinExomeMicrosatellite RepeatsPhenylhydrazinesChicken anemia virusPolymerase Chain ReactionMetabolism, Inborn ErrorsBone Diseases, DevelopmentalPolymorphism, Single-Stranded ConformationalFanconi Anemia Complementation Group C ProteinEye Diseases, HereditaryHeinz BodiesNails, MalformedArabsErythrocyte CountChromosomes, Human, Pair 2Anemia, Diamond-BlackfanAlbinism, OculocutaneousGenetic TestingChromosome DisordersSequence Analysis, DNACharcot-Marie-Tooth Disease