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. 1960 Nov;46(11):1492–1501. doi: 10.1073/pnas.46.11.1492

GENETIC CONTROL OF THE α- AND β-CHAINS OF HEMOGLOBIN*

Harvey A Itano 1, Elizabeth A Robinson 1
PMCID: PMC223072  PMID: 16590776

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. AKSOY M. The hemoglobin E syndromes. II. Sickle-cell-hemoglobin E disease. Blood. 1960 May;15:610–613. [PubMed] [Google Scholar]
  2. ATWATER J., SCHWARTZ R., TOCANTINS L. M. A variety of human hemoglobin with 4 distinct electrophoretic components. Blood. 1960 Jun;15:901–908. [PubMed] [Google Scholar]
  3. HUNT J. A. Identity of the alpha-chains of adult and foetal human haemoglobins. Nature. 1959 May 16;183(4672):1373–1375. doi: 10.1038/1831373a0. [DOI] [PubMed] [Google Scholar]
  4. INGRAM V. M. Separation of the peptide chains of human globin. Nature. 1959 Jun 27;183:1795–1798. doi: 10.1038/1831795a0. [DOI] [PubMed] [Google Scholar]
  5. ITANO H. A. Qualitative and quantitative control of adult hemoglobin synthesis; a multiple allele hypothesis. Am J Hum Genet. 1953 Mar;5(1):34–45. [PMC free article] [PubMed] [Google Scholar]
  6. ITANO H. A., ROBINSON E. Formation of normal and doubly abnormal haemoglobins by recombination of haemoglobin I with S and C. Nature. 1959 Jun 27;183:1799–1800. doi: 10.1038/1831799a0. [DOI] [PubMed] [Google Scholar]
  7. ITANO H. A., ROBINSON E. Properties and inheritance of haemoglobin by asymmetric recombination. Nature. 1959 Nov 7;184:1468–1469. doi: 10.1038/1841468a0. [DOI] [PubMed] [Google Scholar]
  8. Itano H. A., Singer S. J. ON DISSOCIATION AND RECOMBINATION OF HUMAN ADULT HEMOGLOBINS A, S, AND C. Proc Natl Acad Sci U S A. 1958 Jun;44(6):522–529. doi: 10.1073/pnas.44.6.522. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. KUNKEL H. G., BEARN A. G. Minor hemoglobin components of normal human blood. Fed Proc. 1957 Sep;16(3):760–762. [PubMed] [Google Scholar]
  10. RANNEY H. M. Observations on the inheritance of sickle-cell hemoglobin and hemoglobin C. J Clin Invest. 1954 Dec;33(12):1634–1641. doi: 10.1172/JCI103044. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. SCHWARTZ H. C., SPAET T. H., ZUELZER W. W., NEEL J. V., ROBINSON A. R., KAUFMAN S. F. Combinations of hemoglobin G, hemoglobin S and thalassemia occurring in one family. Blood. 1957 Mar;12(3):238–250. [PubMed] [Google Scholar]
  12. SHOOTER E. M., SKINNER E. R., GARLICK J. P., BARNICOT N. A. The electrophoretic characterization of haemoglobin G and a new minor haemoglobin. G2. Br J Haematol. 1960 Apr;6:140–150. doi: 10.1111/j.1365-2141.1960.tb06225.x. [DOI] [PubMed] [Google Scholar]
  13. SMITH E. W., TORBERT J. V. Study of two abnormal hemoglobins with evidence for a new genetic locus for hemoglobin formation. Bull Johns Hopkins Hosp. 1958 Jan;102(1):38–45. [PubMed] [Google Scholar]
  14. Singer S. J., Itano H. A. ON THE ASYMMETRICAL DISSOCIATION OF HUMAN HEMOGLOBIN. Proc Natl Acad Sci U S A. 1959 Feb;45(2):174–184. doi: 10.1073/pnas.45.2.174. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. VON EULER U. S. Exposure to cold and catecholamines. Fed Proc. 1960 Dec;19(Suppl 5):79–81. [PubMed] [Google Scholar]

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