Skip to main content

. 1957 Nov;36(11):1615–1625. doi: 10.1172/JCI103561

Observations on the Minor Basic Hemoglobin Component in the Blood of Normal Individuals and Patients with Thalassemia

H G Kunkel ¹, R Ceppellini ¹, U Müller-Eberhard ¹, J Wolf ¹

PMCID: PMC1072768 PMID: 13475502

1618

Images in this article

Image
on p.1617

Image
on p.1623

Selected References

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

BIANCO I., MONTALENTI G., SILVESTRONI E., SINISCALCO M. Further data on genetics of microcythaemia or thalassaemia minor and Cooley's disease or thalassaemia major. Ann Eugen. 1952 May;16(4):299–315. doi: 10.1111/j.1469-1809.1951.tb02483.x. [DOI] [PubMed] [Google Scholar]
ENG L. I. Postnatal formation of haemoglobin E. Nature. 1956 Nov 10;178(4541):1056–1056. doi: 10.1038/1781056a0. [DOI] [PubMed] [Google Scholar]
ITANO H. A., BERGREN W. R., STURGEON P. The abnormal human hemoglobins. Medicine (Baltimore) 1956 May;35(2):121–159. doi: 10.1097/00005792-195605000-00002. [DOI] [PubMed] [Google Scholar]
KUNKEL H. G., WALLENIUS G. New hemoglobin in normal adult blood. Science. 1955 Aug 12;122(3163):288–288. doi: 10.1126/science.122.3163.288. [DOI] [PubMed] [Google Scholar]
NEEL J. V. The genetics of human haemoglobin differences: problems and perspectives. Ann Hum Genet. 1956 Jul;21(1):1–30. [PubMed] [Google Scholar]
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]
SCHNEIDER R. G., HAGGARD M. E. Sickling, a quantitatively delayed genetic character. Proc Soc Exp Biol Med. 1955 Jun;89(2):196–199. doi: 10.3181/00379727-89-21755. [DOI] [PubMed] [Google Scholar]
SINGER K., CHAPMAN A. Z., GOLDBERG S. R., RUBINSTEIN H. M., ROSENBLUM S. A. Studies on abnormal hemoglobins. IX. Pure (homozygous) hemoglobin C disease. Blood. 1954 Nov;9(11):1023–1031. [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]
SINGER K., CHERNOFF A. I., SINGER L. Studies on abnormal hemoglobins. II. Their identification by means of the method of fractional denaturation. Blood. 1951 May;6(5):429–435. [PubMed] [Google Scholar]
STURGEON P., ITANO H. A., VALENTINE W. N. Chronic hemolytic anemia associated with thalassemia and sickling traits. Blood. 1952 Mar;7(3):350–357. [PubMed] [Google Scholar]
THOMAS E. D., MOTULSKY A. G., WALTERS D. H. Homozygous hemoglobin C disease; report of a case with studies on the pathophysiology and neonatal formation of hemoglobin C. Am J Med. 1955 May;18(5):832–838. doi: 10.1016/0002-9343(55)90195-9. [DOI] [PubMed] [Google Scholar]

ACTIONS

RESOURCES