Flow cytometric measurement of hemoglobin F in RBCs: Diagnostic usefulness in the distinction of hereditary persistence of fetal hemoglobin (HPFH) and hemoglobin S-HPFH from other conditions with elevated levels of hemoglobin F

American Journal of Clinical Pathology

Volumn 117, Issue 6, 2002, Pages 857-863

  Hoyer, James D ^a   Penz, Connie S ^a   Fairbanks, Virgil F ^a   Hanson, Curtis A ^a   Katzmann, Jerry A ^a  

^a MAYO CLINIC   (United States)

Author keywords

Flow cytometry; Hemoglobin F; Hereditary persistence of fetal hemoglobin; HPFH; Kleihauer Betke

Indexed keywords

HEMOGLOBIN F; HEMOGLOBIN S;

ANALYTIC METHOD; ARTICLE; BETA THALASSEMIA; CELLULAR DISTRIBUTION; DELTA BETA THALASSEMIA; DIAGNOSTIC VALUE; ERYTHROCYTE; FLOW CYTOMETRY; GENETIC DISORDER; HEMOGLOBIN DETERMINATION; HEMOGLOBIN SYNTHESIS; HOMOZYGOSITY; HUMAN; KLEIHAUER BETKE ACID ELUTION TEST; MAJOR CLINICAL STUDY; PRIORITY JOURNAL;

ADULT; DIAGNOSIS, DIFFERENTIAL; ERYTHROCYTES; FETAL HEMOGLOBIN; FLOW CYTOMETRY; HEMOGLOBINOPATHIES; HUMANS; INFANT; INFANT, NEWBORN; THALASSEMIA;

EID: 0036261355     PISSN: 00029173     EISSN: None     Source Type: Journal    
DOI: 10.1309/A63X-HG9T-VYG2-X6TX     Document Type: Article

References (14)

1. Deltabeta thalassemia and hereditary persistence of fetal hemoglobin
2. Hereditary persistence of fetal hemoglobin: A study of 79 affected persons in 15 Negro families in Baltimore
3. The Negro variety of hereditary persistence of fetal haemoglobin is a mild form of thalassaemia
4. The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobases
5. 0gamma type of hereditary persistence of fetal hemoglobin with beta chain production in cis
6. 0gamma gene
7. Genetic heterogeneity in heterocellular hereditary persistence of fetal hemoglobin
8. Demonstration von fetalem hamoglobin in der erythrocyten eines blutausstrichs
9. Semi-quantitative estimation of the distribution of fetal hemoglobin in red cell populations
10. Hereditary persistence of foetal hemoglobin production, and its interaction with the sickle-cell trait
11. A new form of hereditary persistence of fetal hemoglobin and its association with sickle cell trait
12. Sickle cell trait/hereditary persistence of fetal hemoglobin trait: Misdiagnosis as sickle cell anemia by newborn screening
13. Sickle cell-hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromes
14. Detection of fetal red cells in fetomaternal hemorrhage using a fetal hemoglobin monoclonal antibody by flow cytometry