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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- DITTMAN W. A., HAUT A., WINTROBE M. M., CARTWRIGHT G. E. Hemoglobin H associated with an uncommon variant of thalassemia trait. Blood. 1960 Jul;16:975–983. [PubMed] [Google Scholar]
- FLATZ G., PIK C., SRINGAM S. HAEMOGLOBINOPATHIES IN THAILAND. I. A STUDY OF PATIENTS WITH THE THALASSAEMIA SYNDROME AND THEIR FAMILIES. Br J Haematol. 1965 Mar;11:216–226. doi: 10.1111/j.1365-2141.1965.tb06581.x. [DOI] [PubMed] [Google Scholar]
- KUNKEL H. G., CEPPELLINI R., MULLER-EBERHARD U., WOLF J. Observations on the minor basic hemoglobin component in the blood of normal individuals and patients with thalassemia. J Clin Invest. 1957 Nov;36(11):1615–1625. doi: 10.1172/JCI103561. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LIE-INJO L. E. Alpha-chain thalassemia and hydrops fetalis in Malaya: report of five cases. Blood. 1962 Nov;20:581–590. [PubMed] [Google Scholar]
- SINGER K., CHERNOFF A. I., SINGER L. Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation. Blood. 1951 May;6(5):413–428. [PubMed] [Google Scholar]
- ZUELZER W. W., ROBINSON A. R., BOOKER C. R. Reciprocal relationship of hemoglobins A2 and F in beta chain thalassemias, a key to the genetic control of hemoglobin F. Blood. 1961 Apr;17:393–408. [PubMed] [Google Scholar]