Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional α-globin and β-globin gene

Haematologica

Volumn 86, Issue 4, 2001, Pages 363-367

  Traeger Synodinos, J ^a   Papassotiriou, I ^a   Vrettou, C ^a   Skarmoutsou, C ^a   Stamoulakatou, A ^a   Kanavakis, E ^a  

^a UNIVERSITY OF ATHENS   (Greece)

Author keywords

Bone marrow activity; Complex genotype; Functional anemia; HbH disease; Heterozygous thalassemia

Indexed keywords

2,3 DIPHOSPHOGLYCERIC ACID; ALPHA GLOBIN; BETA GLOBIN; ERYTHROPOIETIN; HEMOGLOBIN A2; HEMOGLOBIN H; OXYGEN; TRANSFERRIN RECEPTOR;

ADOLESCENT; ADULT; ARTICLE; BETA THALASSEMIA; BLOOD LEVEL; BONE MARROW; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; ERYTHROCYTE; ERYTHROID CELL; FEMALE; GENOTYPE; HUMAN; HUMAN CELL; HYPOXEMIA; INFANT; IRON DEFICIENCY ANEMIA; MALE; OXYGEN AFFINITY; PHENOTYPE;

ADOLESCENT; ADULT; ALPHA-THALASSEMIA; ANEMIA; BETA-THALASSEMIA; BONE MARROW; CHILD; CHILD, PRESCHOOL; FAMILY HEALTH; FEMALE; GENOTYPE; GLOBINS; HETEROZYGOTE; HUMANS; INFANT; MALE; PHENOTYPE; RETICULOCYTES;

EID: 0035025401     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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