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Research Article

Diagnostic Criteria of Thalassemia

Pages 116-120 | Published online: 27 Sep 2008

References

  • Fessas P. Inclusions of hemoglobin in erythroblasts and erythrocytes in thalassemia. Blood 1963; 21: 21
  • Kattamis C., Lehmann H. The genetical interpretation of hemoglobin H disease. Hum. Hered. 1970; 20: 156
  • Kattamis C., Lehmann H. Duplication of alpha-thalassemia gene in three Greek families with haemoglobin H disease. Lancet 1970; 2: 635
  • Kattamis C., Lagos P., Metaxotou-Mavtomati A., Matsaniotis N. Serum iron and unsaturated iron binding capacity in the α-thalassemia trait: their relation to the levels of hemoglobins A, A2 and F. J. Med. Genet. 1972; 9: 154
  • Kattamis C., Metaxotou-Mavtomati A., Katamboula K., Nasika E., Lehmann H. The clinical and hematologic findings in children inheriting two types of thalassemia: β(A2) and high F variant of δβ3(F). Br. J. Haematol. 1973; 25: 375
  • Lehmann H., Carrell R. W. Differences between α and β chain mutants of human haemoglobin and between αand β thalassaemia. Possible duplication of α chain gene. Br. Med. J. 1968; 4: 748
  • Stamatoyannopoulos G., Fessas P., Papayannopoulou T. F-thalassemia: a study of thirty-one families with simple heterozygotes and combinations of F-thalassemia with A2 thalassemia. Am. J. Med. 1969; 47: 194
  • Wasi P., Na-Nakorn S., Pootiakul S., Sookanet M., Ditsthasongchan P., Poinpatkul M., Panich Y. Alpha and beta thalassemia in Thailand. Ann. N. Y. Acad. Sci. 1968; 165: 60

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