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Hemoglobin

international journal for hemoglobin research

Volume 4, 1980 - Issue 3-4

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Original Article

Adult and Fetal Hemoglobin Production in Erythroid Colonies from Subjects with β-Thalassemia or with Hereditary Persistence of Fetal Hemoglobin (HPFH)

T. H. J. Huisman Laboratory of Protein Chemistry and Comprehensive Sickle Cell Center Department of Cell and Molecular Biology, Medical College of Georgia Augusta, Georgia, 30912

A. L. Reese Laboratory of Protein Chemistry and Comprehensive Sickle Cell Center Department of Cell and Molecular Biology, Medical College of Georgia Augusta, Georgia, 30912

M. E. Gravely Laboratory of Protein Chemistry and Comprehensive Sickle Cell Center Department of Cell and Molecular Biology, Medical College of Georgia Augusta, Georgia, 30912

J. B. Wilson Laboratory of Protein Chemistry and Comprehensive Sickle Cell Center Department of Cell and Molecular Biology, Medical College of Georgia Augusta, Georgia, 30912

B. Webber Laboratory of Protein Chemistry and Comprehensive Sickle Cell Center Department of Cell and Molecular Biology, Medical College of Georgia Augusta, Georgia, 30912

A. E. Felice Laboratory of Protein Chemistry and Comprehensive Sickle Cell Center Department of Cell and Molecular Biology, Medical College of Georgia Augusta, Georgia, 30912

Pages 449-467 | Published online: 07 Jul 2009

Cite this article
https://doi.org/10.3109/03630268008996226

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Adult and Fetal Hemoglobin Production in Erythroid Colonies from Subjects with β-Thalassemia or with Hereditary Persistence of Fetal Hemoglobin (HPFH)

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Adult and Fetal Hemoglobin Production in Erythroid Colonies from Subjects with β-Thalassemia or with Hereditary Persistence of Fetal Hemoglobin (HPFH)

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