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Hemoglobin
international journal for hemoglobin research
Volume 3, 1979 - Issue 5
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Original Article

Microchromatographic Quantitation of Fetal Hemoglobin in Patients with Sickle Cell Disease

E. C. Abraham Department of Cell and Molecular Biology and the Sickle Cell Center, Medical College of Georgia, Augusta, Georgia, 30912
,
J. Carver Department of Cell and Molecular Biology and the Sickle Cell Center, Medical College of Georgia, Augusta, Georgia, 30912
,
J. Döbler Department of Cell and Molecular Biology and the Sickle Cell Center, Medical College of Georgia, Augusta, Georgia, 30912
,
P. F. Milner Department of Cell and Molecular Biology and the Sickle Cell Center, Medical College of Georgia, Augusta, Georgia, 30912
&
T. H. J. Huisman Department of Cell and Molecular Biology and the Sickle Cell Center, Medical College of Georgia, Augusta, Georgia, 30912
Pages 341-351 | Received 30 Apr 1979, Accepted 19 Jul 1979, Published online: 07 Jul 2009

Citations (8)

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Read on this site (2)

Georgi D. Efremov. (2001) FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999). Hemoglobin 25:2, pages 125-168.
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William L. Marsh & Harold M. Koenig. (1982) The Laboratory Evaluation of Microcytic Red Blood Cells. CRC Critical Reviews in Clinical Laboratory Sciences 16:3, pages 195-254.
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Articles from other publishers (6)

A. D. Adekile & T. H. J. Huisman. (1993) Hb F in sickle cell anemia. Experientia 49:1, pages 16-27.
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A. E. Felice, K. M. McKie, M. P. Cleek, E. M. Marino, A. Kutlar & V. C. McKie. (2006) Effects of α‐thalassemia‐2 on the developmental changes of hematological values in children with sickle cell disease from georgia. American Journal of Hematology 25:4, pages 389-400.
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Jonathan S. Krauss, Mary H. Jonah, Charles R. Baisden, Denyse Y. Parnell, Ann E. Neely & Patricia Mohorn. (1985) The microchromatographic measurement of fetal hemoglobin levels in hemoglobin C-associated conditions. Clinical Biochemistry 18:4, pages 252-253.
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M. M. Elseweidy & E. C. Abraham. (2006) The relationship between fetal hemoglobin level and glycosylation in sickle cell disease. American Journal of Hematology 16:4, pages 375-381.
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M.E. Headlee, M.B. Gardiner, A.L. Reese & T.H.J. Huisman. (1983) The distribution of fetal hemoglobin and the types of γ chain in red cell fractions separated by gradient centrifugation from blood of patients with sickle cell anemia and other hemoglobinopathies. Biochemical Medicine 29:3, pages 337-354.
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P. Basset, F. Braconnier & J. Rosa. (1982) An update on electrophoretic and chromatographic methods in the diagnosis of hemoglobinopathies. Journal of Chromatography B: Biomedical Sciences and Applications 227:2, pages 267-304.
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