Full text
PDF









Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- APTHORP G. H., MEASDAY B., LEHMANN H. Pregnancy in sickle-cell anaemia. Lancet. 1963 Jun 22;1(7295):1344–1346. doi: 10.1016/s0140-6736(63)91924-x. [DOI] [PubMed] [Google Scholar]
- BETKE K., KLEIHAUER E. Fetaler und bleibender Blutfarbstoff in Erythrozyten und Erythroblasten von menschlichen Feten und Neugeborenen. Blut. 1958 Nov;4(5):241–249. doi: 10.1007/BF01630321. [DOI] [PubMed] [Google Scholar]
- BREWER G. J., TARLOV A. R., ALVING A. S. Methaemoglobin reduction test: a new, simple, in vitro test for identifying primaquine-sensitivity. Bull World Health Organ. 1960;22:633–640. [PMC free article] [PubMed] [Google Scholar]
- BUCHANAN K. D., KINLOCH J. D., HUTCHISON H. E., PINKERTON P. H., CASSIDY P. THALASSAEMIA IN SCOTS. J Clin Pathol. 1963 Nov;16:596–600. doi: 10.1136/jcp.16.6.596. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CURTIS E. M. Pregnancy in sickle cell, anemia, sickle cell-hemoglobin C disease, and variants thereof. Am J Obstet Gynecol. 1959 Jun;77(6):1312–1323. doi: 10.1016/0002-9378(59)90373-4. [DOI] [PubMed] [Google Scholar]
- EISENSTEIN M. I., FRIEDMAN S., POSNER A. C. Sickle-cell anemia in pregnancy; a review of the literature with additional case histories. Am J Obstet Gynecol. 1956 Sep;72(3):622–634. [PubMed] [Google Scholar]
- 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]
- RAPER A. B., GAMMACK D. B., HUEHNS E. R., SHOOTER E. M. Four haemoglobins in one individual. A study of the genetic interaction of Hb-G and Hb-C. Br Med J. 1960 Oct 29;2(5208):1257–1261. doi: 10.1136/bmj.2.5208.1257. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROBERTS P. D. THE THALASSAEMIA TRAIT IN AN ENGLISH FAMILY. J Clin Pathol. 1963 Nov;16:593–595. doi: 10.1136/jcp.16.6.593. [DOI] [PMC free article] [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]
- SMITH C. H., ERLANDSON M. E., STERN G., SCHULMAN I. The role of splenectomy in the management of thalassemia. Blood. 1960 Feb;15:197–211. [PubMed] [Google Scholar]
- TARLOV A. R., BREWER G. J., CARSON P. E., ALVING A. S. Primaquine sensitivity. Glucose-6-phosphate dehydrogenase deficiency: an inborn error of metabolism of medical and biological significance. Arch Intern Med. 1962 Feb;109:209–234. doi: 10.1001/archinte.1962.03620140081013. [DOI] [PubMed] [Google Scholar]
- ZINKHAM W. H. Peripheral blood and bilirubin values in normal full-term primaquine-sensitive Negro infants: effect of vitamin K. Pediatrics. 1963 Jun;31:983–995. [PubMed] [Google Scholar]