AllisonA. C. (1960). Glucose-6-phosphate dehydrogenase deficiency in red blood cells of East Africans. Nature, Lond., 186, 531.
2.
AllisonA. C. (1965). Population genetics of abnormal haemoglobins and gIucose-6-phosphate dehydrogenase deficiency. In ‘Abnormal haemoglobins in Africa’; a C.I.O.M.S. symposium—Edit. JonxisJ. H. P., Blackwell Scientific Publications, Oxford: pp. 365–391.
3.
AlvingA. S.KellermeyerR. W.TarlovA.SchrierS.CarsonP. E. (1958). Biochemical and genetic aspects of primaquine-sensitive hemolytic anemia. Ann. int. Med., 49, 240.
4.
BeutlerE.DernR. J.AlvingA. S. (1955). The hemolytic effect of primaquine. VI. An in vitro test for sensitivity of erythrocytes to primaquine. J. Lab. clin. Med., 45, 40.
5.
BeutlerE.RobsonM. J.ButternwieserE. (1957). The glutathione instability of drug-sensitive red cells. J. Lab. clin. Med., 49, 84.
6.
BeutlerE. (1960). Drug-induced hemolytic anemia (primaquine sensitivity). In “The metabolic basis of inherited disease”. Eds. StanburyJ. B.WyngardenJ. B.FredricksonD. S.New York: McGraw-Hill Book Co. Inc., pp. 1031–1067.
7.
BlackburnE. K.LorberJ. (1963). Chronic haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency. Proc. R. Soc. Med., 56, 505.
8.
BowdlerA. J.PrankerdT. A. J. (1964). Studies in congenital non-spherocytic haemolytic anaemias with specific enzyme defects. Acta haemat., 31, 65.
9.
BroadribbH. S.WorssamA. R. (1961). Favism in an Englishwoman. Brit. med. J., 1, 1367.
10.
ChildsB.ZinkhamW.BrowneE. A.KimbroE. L.TorbertJ. V. (1958). A genetic study of a defect in glutathione metabolism of the erythrocyte. Bull. Johns Hopkins Hosp., 102, 21.
11.
CrosbyW. H. (1956). Newsletter—Favism in Sardinia. Blood, 11, 91.
12.
DernR. J.WeinsteinI. M.LeroyG. V.TalmageD. W.AlvingA. S. (1954). The hemolytic effect of primaquine. I. The localization of the drug-induced hemolytic defect in primaquine-sensitive individuals. J. Lab. clin. Med., 43, 303.
13.
EdingtonG. M.Watson-WilliamsE. J. (1965). Sickling, haemoglobin C, glucose-6-phosphate dehydrogenase deficiency and malaria in western Nigeria. In ‘Abnormal haemoglobins in Africa’. A C.I.O.M.S. symposium—Edit. JonxisJ. H. P.Oxford: Blackwell Scientific Publications, pp. 393–401.
14.
FairbanksV. F.BeutlerE. (1962). A simple method for detection of erythrocyte glucose-6-dehydrogenase deficiency (G-6-PD Spot Test). Blood, 20, 591.
GillesH. M.TaylorB. G. (1961). The existence of the glucose-6-phosphate dehydrogenase deficiency trait in Nigeria and its clinical implications. Ann. trop. Med. and Parasit., 55, 64.
17.
HarrisR.GillesH. M. (1961). Glucose-6-phosphate dehydrogenase deficiency in the peoples of the Niger delta. Ann. hum. Gen., 25, 199.
18.
KirkmanH. N.BrinsonG. A.PickardB. M. (1963). New variants of glucose-6-phosphate dehydrogenase in Caucasian males. Proc. IX. Europ. Congr. Haematology.Basle: Karger, pp. 685–688.
19.
LyonM. F. (1961). Gene action in the X-chromo-somes of the mouse. Nature, Lond., 190, 372.
20.
MohlerD. N.CrockettC. L.Jr. (1964). Hereditary hemolytic disease secondary to glucose-6-phosphate dehydrogenase; Report of three cases with special emphasis on ATP metabolism. Blood, 23, 427.
21.
MotulskyA. G.Campbell-KrautJ. M. (1961). Population genetics of glucose-6-phosphate dehydrogenase deficiency of the red cell. In ‘Proceedings of the Conference on Genetic Polymorphisms and Geographic Variations in Disease’. Edit. BlumbergB. S.New York: Grune and Stratton, pp. 159–180.
22.
MotulskyA. G. (1965). Theoretical and clinical problems of glucose-6-phosphate dehydrogenase deficiency. Its occurrence in Africans and its combination with hemoglobinopathy. In ‘Abnormal haemoglobins in Africa’. A C.I.O.M.S. symposium. Edit.: JonxisJ. H. P.Oxford: Blackwell Scientific Publications, pp. 143–196.
23.
NewtonW. A.Jr.BassJ. C. (1958). Glutathione-sensitive chronic non-spherocytic hemolytic anemia. Amer. J. Dis. Child., 96, 501.
PanizonF.ZacchelloF. (1965). The mechanism of haemolysis in favism: Some analogy in the activity of primaquine and fava juice. Acta haemat., 33, 129.
26.
PorterI. H.BoyerS. H.Watson-WilliamsE. J.AdamA.SzejnbergA.SiniscalcoM. (1964). Variations of glucose-6-phosphate dehydrogenase in different populations. Lancet, 1, 895.
27.
RamotB.AshkenaziI.RimonA.AdamA.ShebaC. (1961). Activation of glucose-6-phosphate dehydrogenase of enzyme-deficient subjects: II. Properties of the activator and the activation reaction. J. clin. Invest., 40, 611.
28.
SartoriE.PanizonF.ZacchelloF. (1966). Bimodal distribution of erythrocytes in heterozygotes for strong mediterranean glucose-6-phosphate dehydrogenase deficiency. J. med. Genet., 3, 42.
29.
ShahidiN. T.DiamondL. K. (1959). Enzyme deficiency in erythrocytes in congenital non-spherocytic hemolytic anemia. Pediatrics, 24, 245.
SzejnbergA.ShebaC.AdamA. (1958). Selective occurrence of glutathione instability in red blood corpuscles of the various Jewish tribes. Blood, 13, 1043.
32.
SzejnbergA.ShebaC.RamotB.AdamA. (1960). Differences in hemolytic susceptibility among subjects with glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. Clin. Res., 8, 18.
33.
WeatherallD. J. (1960). Enzyme deficiency in haemolytic disease of the newborn. Lancet, 2, 835.
34.
ZinkhamW. H.LenhardR. E.ChildsB. (1958). A deficiency of glucose-6-phosphate dehydrogenase activity in erythrocytes from patients with favism. Bull. Johns Hopkins Hosp., 102, 169.