Artigo Revisado por pares

The Sickle Cell Trait in Africa

1953; Wiley; Volume: 55; Issue: 5 Linguagem: Inglês

10.1525/aa.1953.55.5.02a00040

ISSN

1548-1433

Autores

Ronald Singer,

Tópico(s)

Iron Metabolism and Disorders

Resumo

American AnthropologistVolume 55, Issue 5 p. 634-648 The Sickle Cell Trait in Africa RONALD SINGER, RONALD SINGER University of Cape Town Mowbray, Cape Province, South AfricaSearch for more papers by this author RONALD SINGER, RONALD SINGER University of Cape Town Mowbray, Cape Province, South AfricaSearch for more papers by this author First published: December 1953 https://doi.org/10.1525/aa.1953.55.5.02a00040Citations: 11AboutPDF ToolsExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL BIBLIOGRAPHY Abdoosh, V. B. and S. El-Dewi 1949 The blood groups of Egyptians. 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Société de Biologie 143: 579– 581. Jeffreys, M. D. W. 1953 Personal communication. Jelliffe, D. B. and J. Humphreys 1952 The sickle cell trait in western Nigeria. British Medical Journal 1: 405– 406. Keane, A. H. 1920 Man: Past and Present. Cambridge University Press, London. Lambotte-Legrand, J. and Lambotte-Legrand, C. 1951 L'anémie à hématies falciformes chez l'enfant indigène du Bas-Congo. Annales Société Belge de Médecine Tropicale 31: 207– 234. Lancet June 30, 1951 Inherited red cell anomalies. Vol. 261: 1400– 1402. Lehmann, H. 1951 Sickle-cell anaemia and sickle-cell trait as homozygous and heterozygous gene-combinations. Nature 167: 931– 932. London. Lehmann, H. 1952 Sickle-cell anomaly in Greece. Lancet 262: 1068. Lehmann, H. and M. Cutbush 1952 Sickle-cell trait in southern India. British Medical Journal 1: 404– 405. Lehmann, H. and A. B. Raper 1949 Distribution of sickle-cell trait in Uganda, and its ethnological significance. Nature 164: 494– 495.London. Lundman, B. 1948 Geography of human blood broups (A, B, O system). Evolution 2: 231– 237. Makrycostas, K. 1940 Über die Sichelzellanämie. Wiener Archivo für Innere Medizin 33: 330– 342, 390–398. Berlin. McGavack, T. H. and W. M. German 1944 Sicklemia in Black Carib Indian. American Journal of the Medical Sciences 208: 350– 355. Mera, B. 1943 Preliminares del estudio de la meniscocitemia en Colombia. Boletín de la Oficina Sanitaria Panamericana 22: 680– 682. Miyamoto, K. and J. H. Korb 1927 Meniscocytosis (latent sickle cell anemia); its incidence in St. Louis. Southern Medical Journal 20: 912– 916. Neel, J. V. 1947 The clinical detection of the genetic carriers of inherited disease. Medicine 26: 115– 153. Neel, J. V. 1949 The inheritance of sickle cell anemia. Science 110: 64– 66. Neel, J. V. 1951 The inheritance of the sickling phenomenon, with particular reference to sickle cell disease. Blood 6: 389– 412. Neel, J. V. 1952 Perspectives in the genetics of sickle cell disease. Blood 7: 467– 472. Neel, J. V., I. C. Wells and H. A. Itano 1951 Familial differences in the proportion of abnormal hemoglobin present in the sickle cell trait. Journal of Clinical Investigation 30: 1120– 1124. Parent, J. 1950 Sickle cell anemia. Annales Société Belge de Médecine Tropicale 30: 47– 52. Pauling, L., H. A. Itano, S. J. Singer and I. C. Wells 1949 Sickle-cell anemia, a molecular disease. Science 110: 543– 548. Powell, W. N., J. G. Rodarte and J. V. Neel 1950 The occurrence in a family of Sicilian ancestry of the traits for both sickling and thalassemia. Blood 5: 887– 897. Raper, A. B. 1949 The incidence of sicklaemia. East African Medical Journal 26: 281– 282. Raper, A. B. 1950 Sickle-cell disease in Africa and America—a comparison. Journal of Tropical Medicine and Hygiene 53: 49– 53. Shapiro, M. 1951a The ABO, P and Rh blood group systems in the South African Bantu. South African Medical Journal 25: 165– 170, 187–192. Shapiro, M. 1951b Further evidence of homogeneity of blood group distribution in the South African Bantu. South African Medical Journal 25: 406– 411. Silvestroni, E., I. Bianco, G. Montalenti and M. Siniscalco 1950 Frequency of microcythaemia in some Italian districts. Nature 165: 682– 683.London. Singer, K. and B. Fisher 1952 The distribution of Type S (sickle cell) hemoglobin and Type F (alkali resistant) hemoglobin within the red cell population in sickle cell anemia. Blood 7: 1216– 1226. Singer, K., S. Robin, J. C. King and R. N. Jefferson 1948 The life span of the sickle cell, and the pathogenesis of sickle cell anemia. Journal of Laboratory and Clinical Medicine 33: 975– 984. Singer, R. 1953 The origin of the sickle cell. South African Journal of Science. In Press. Sydenstricker, V. P. 1924 Further observations on sickle-cell anemia. Journal of the American Medical Association 83: 12– 17. Taliaferro, W. H. and J. G. Huck 1923 The inheritance of sickle cell anemia in man. Genetics 8: 594– 598. Wiener, A. S. 1946 Recent developments in knowledge of Rh-Hr blood types; tests for Rh sensitization. American Journal of Clinical Pathology 16: 477– 497. Williams, A. W. and J. P. Mackey 1949 Rapid determination of the sickle cell trait by the use of a reducing agent. Journal of Clinical Pathology 2: 141– 142. Wintrobe, M. M. 1946 Clinical hematology. 2nd ed. (p. 501). Lea and Febiger, Philadelphia. Wright, F. J., and A. W. Pearson 1949 Sickle cell anaemia in an Indian family. East African Medical Journal 26: 255– 259. Zaberdinos, A. 1950 Quoted by Choremis et al. (see above). Zoutendyck, A. 1947 Rhesus factor blood types in South African Bantu. South African Journal of Medical Sciences 12: 167– 169. Citing Literature Volume55, Issue5December 1953Pages 634-648 ReferencesRelatedInformation

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