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Original Articles

Hemoglobins and Heredity

Second of Two Parts

, M.D. (EDITOR) & , M.D.
Pages 91-94 | Published online: 18 Apr 2016

REFERENCES

  • Conley, C. L. and Charache, S.: Mechanisms by which some abnormal hemoglobins produce clinical manifestations. Seminars Hemat 4:53–71 (January) 1967.
  • Diggs, L. W.: Sickle cell crises. Amer J Clin Path 44:1, 1965.
  • Heller, P.: Hemoglobinopathic dysfunction of the red cell. Amer J Med 41:799, 1966.
  • Ingram, V. M.: The Hemoglobins in Genetics and Evolution. New York, Columbia University Press, 1963.
  • JaffÉ, E. R. and Heller, P.: Methemoglobinemia in man. In Moore, C. V. and Brown, E. B. (Editors): Progress in Hematology. New York, Grune & Stratton, Inc., 1964, vol 4, p 48.
  • Lehmann, H. and Huntsman, R. G.: Man's Haemoglobins. Philadelphia, J. B. Lippincott Company, 1966.
  • Nathan, D. G. and Gunn, R. B.: Thalassemia: The consequences of unbalanced hemoglobin synthesis. Ibid.,3 p 815.
  • Riggs, A.: Functional properties of hemoglobins. Physiol Rev 45:619, 1965.
  • Weatherall, D. J.: The thalassemias. Ibid.,1 p 72.

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