Fetal hemoglobin expression in the compound heterozygous state for -117 (G→A) (A)γ HPFH and IVS-1 nt 110 (G→A) β+ thalassemia: A case study

European Journal of Haematology

Volumn 65, Issue 2, 2000, Pages 93-96

  Dedoussis, G V Z ^a,b   Sinopoulou, K ^a   Gyparaki, M ^a   Loutradis, A ^a  

^a LAIKO GENERAL HOSPITAL   (Greece)

^b HAROKOPIO UNIVERSITY   (Greece)

Author keywords

Beta globin mutation; Haplotype; Hereditary persistence of fetal hemoglobin (HPFH); Thalassaemia; Xmn I

Indexed keywords

HEMOGLOBIN F;

ADULT; ARTICLE; BETA THALASSEMIA; CASE REPORT; FEMALE; GENE MUTATION; GENOTYPE; HEMOGLOBIN SYNTHESIS; HUMAN; MALE; PRIORITY JOURNAL; PROTEIN EXPRESSION;

ADULT; BASE SEQUENCE; BETA-GLOBULINS; BETA-THALASSEMIA; FEMALE; FETAL HEMOGLOBIN; HAPLOTYPES; HEMOGLOBIN A2; HETEROZYGOTE; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; POINT MUTATION; PROMOTER REGIONS (GENETICS); RNA SPLICING;

EID: 0033868702     PISSN: 09024441     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-0609.2000.90121.x     Document Type: Article

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