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- BEUTLER E., YEH M. K., NECHELES T. Incidence of the erythrocytic defect associated with drug-sensitivity among oriental subjects. Nature. 1959 Mar 7;183(4662):684–685. doi: 10.1038/183684b0. [DOI] [PubMed] [Google Scholar]
- GROSS R. T., HURWITZ R. E., MARKS P. A. An hereditary enzymatic defect in erythrocyte metabolism: glucose-6-phosphage dehydrogenase deficiency. J Clin Invest. 1958 Aug;37(8):1176–1184. doi: 10.1172/JCI103707. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MOTULSKY A. G. Metabolic polymorphisms and the role of infectious diseases in human evolution. Hum Biol. 1960 Feb;32:28–62. [PubMed] [Google Scholar]
- SHIH L. Y., LEE T. C. Glucose-6-phosphate dehydrogenase dye test on patients and their family members of acute hemolytic anemia. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1961 Apr-Jun;2:106–112. [PubMed] [Google Scholar]
- STEVENSON T. D., McDONALD B. L., ROSTON S. Colorimetric method for determination of erythrocyte glutathione. J Lab Clin Med. 1960 Jul;56:157–160. [PubMed] [Google Scholar]
- VELLA F. Susceptibility to drug-induced haemolysis in Singapore. Med J Malaya. 1959 Jun;13:298–308. [PubMed] [Google Scholar]
- WEATHERALL D. J. Enzyme deficiency in haemolytic disease of the newborn. Lancet. 1960 Oct 15;2(7155):835–837. doi: 10.1016/s0140-6736(60)91904-8. [DOI] [PubMed] [Google Scholar]
- ZINKHAM W. H., LENHARD R. E., Jr, CHILDS B. A deficiency of glucose-6-phosphate dehydrogenase activity in erythrocytes from patients with favism. Bull Johns Hopkins Hosp. 1958 Apr;102(4):169–175. [PubMed] [Google Scholar]