References
Baup, H.: Fréquence de l'hémoglobine E au Laos. Med. trop. 24, 51–60 (1964)
Benesch, R., MacDuff, G., Benesch, R. E.: Determination of oxygen equilibrium with a versatile new tonometer. Anal. Biochem. 112, 81–87 (1965)
Blomback, M., Blomback, B., Memmen, E. F., Prasad, A. S.: Fibrinogen Detroit, a molecular defect in the N-terminal disulfide knot of human fibrinogen? Nature 218, 134–137 (1968)
Capp, G. L., Rigas, D. A., Jones, R. T.: Evidence for a new haemoglobin chain (ζ-chain). Nature 228, 278–280 (1970)
Clegg, J. B., Naughton, M. A., Weatherall, D. J.: Abnormal human haemoglobins: separation and characterization of the α- and β-chains by chromatography, and the determination of two new variants, Hb Chesapeake and Hb J (Bangkok). J. Mol. Biol. 19, 91–108 (1966)
De Jong, W. W., Khan, P. M., Bernini, L. F.: Hemoglobin Koya Dora; high frequency of a chain termination mutant. Am. J. Hum. Genet. 27, 81–89 (1975)
Drysdale, J. W., Righetti, P. G., Bunn, H. F.: The separation of human and animal hemoglobins by isoelectric focusing in polyacrylamide gel. Biochim. Biophys. Acta 229, 42–50 (1971)
Lie-Injo Luan Eng, Duraisamy, G.: The slow moving haemoglobin X components in Malaysians. Hum. Hered. 22, 118–123 (1972)
Lingrel, J. B., Borsook, H.: A comparison of amino-acid incorporation into the hemoglobin and ribosomes of narrow erythroid cells and circulating erythrocytes of severely anemic rabbits. Biochemistry 2, 309–314 (1963)
Marengo-Rowe, A. J.: Rapid electrophoresis and quantitation of haemoglobins on cellulose acetate. J. Clin. Pathol. 18, 790–792 (1965)
Milner, P. F., Clegg, J. B., Weatherall, D. J.: Haemoglobin H disease due to a unique haemoglobin variant with an elongated α-chain. Lancet 1971 I, 729–732
Minnich, V., Hill, R. J., Khuri, P. D., Anderson, M. E.: Hemoglobin Hope; a beta chain variant. Blood 25, 830–838 (1965)
Na-Nakorn, S., Wasi, P.: Alpha thalassemia in Northern Thailand. Am. J. Hum. Genet. 22, 645–651 (1970)
Pagnier, J., Wajcman, H., Labie, D.: Defect in hemoglobin synthesis possibly due to a disturbed association. FEBS Lett. 45, 252–255 (1974)
Pootrakul, S., Wasi, P., Pornpatkul, M., Na-Nakorn, S.: Incidence of alpha-thalassemia in Bangkok. J. Med. Assoc. Thai. 53, 250 (1970)
Pootrakul, S., Wasi, P., Na-Nakorn, S.: cited in: Weatherall and Clegg (1975)
Sicard, D., Kaplan, J. C., Labie, D.: Haemoglobinopathies and G-6-PD deficiency in Laos. Lancet 1978 II, 571–572
Thillet, J., Caburi, J., Brun, B., Cohen-Solal, M., Garel, M. C., N'Go Minh, M., Rosa, J.: Abnormal functional properties of Hb Hope α2β2 (H14) Gly→Asp: a low oxygen affinity hemoglobin with decreased DPG effect. FEBS Lett. 47, 47–52 (1974)
Tuchinda, S., Rucknagel, D. L., Minnich, V., Boonyaprakob, U., Balankura, K., Suvatee, V.: The coexistence of the genes for hemoglobin E and thalassemia in Thais, with resultant suppression of hemoglobin E synthesis. Am. J. Hum. Genet. 16, 311–320 (1964)
Tuchinda, S., Beale, D., Lehmann, H.: The suppression of haemoglobin E synthesis. When haemoglobin H disease and haemoglobin E trait occur together. Humangenetik 3, 312–318 (1967)
Wasi, P., Na-Nakorn, S., Suingdumrong, A.: Study of the distribution of haemoglobin E, thalassemias and G-6-PD deficiency in Northeastern Thailand. Nature 214, 501 (1967)
Wasi, P., Na-Nakorn, S., Pootrakul, S., Sookanek, M., Disthasongchan, P., Pornpatkul, M., Panich, V.: Alpha- and beta-thalassemia in Thailand. Ann. NY Acad. Sci. 165, 60–82 (1969)
Wasi, P., Na-Nakorn, S., Pootrakul, S.:The α-thalassemias. Clin. Haematol. 3, 383 (1974)
Weatherall, D. J.: Abnormal haemoglobins in the neonatal period and their relationship to thalassemia. Br. J. Haematol. 9, 265–277 (1963)
Weatherall, D. J., Clegg, J. B.: The thalassemia syndromes, 2nd ed. Oxford: Blackwell Scientific Publications 1972
Weatherall, D. J., Clegg, J. B.: The α-chain termination mutants and their relation to the α-thalassemias. Philos. Trans. R. Soc. Lond. [Biol.] 271, 411–455 (1975)
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Sicard, D., Lieurzou, Y., Lapoumeroulie, C. et al. High genetic polymorphism of hemoglobin disorders in Laos. Hum Genet 50, 327–336 (1979). https://doi.org/10.1007/BF00399399
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DOI: https://doi.org/10.1007/BF00399399