H Lehmann, A Lang. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdultAfrican Continental Ancestry GroupAnemia, Sickle Cell/complicationsCell SurvivalChildCrossing Over, GeneticErythrocyte CountErythrocytesFemaleFetal Hemoglobin/analysisGenesGenetic LinkageGenetic VariationGlobins/biosynthesisHematocritHemoglobin HHemoglobinopathies/geneticsHemoglobinsHemoglobins, Abnormal/analysisHeterozygoteHomozygoteHumansInclusion BodiesIron/bloodOsmotic FragilityPeptide Fragments/biosynthesisThalassemia/complicationsThalassemia/diagnosisThalassemia/genetics
Substances: See more » HemoglobinsHemoglobins, AbnormalPeptide FragmentsGlobinsFetal HemoglobinHemoglobin HIron
Year: 1974 PMID: 4370548 DOI: 10.1111/j.1749-6632.1974.tb20580.x
Source DB: PubMed Journal: Ann N Y Acad Sci ISSN: 0077-8923 Impact factor: 5.691