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. 1973 Jul;25(4):382–387.

Hemoglobin Constant Spring (slow-moving hemoglobin X components) and hemoglobin e in Malayan aborigines.

L I Eng, A Baer, A N Lewis, Q B Welch
PMCID: PMC1762457  PMID: 4716657

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Clegg J. B., Weatherall D. J., Milner P. F. Haemoglobin Constant Spring--a chain termination mutant? Nature. 1971 Dec 10;234(5328):337–340. doi: 10.1038/234337a0. [DOI] [PubMed] [Google Scholar]
  2. Efremov G. D., Wrightstone R. N., Huisman T. H., Schroeder W. A., Hyman C., Ortega J., Williams K. An unusual hemoglobin anomaly and its relation to alpha-thalassemia and hemoglobin-H disease. J Clin Invest. 1971 Aug;50(8):1628–1636. doi: 10.1172/JCI106651. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Eng L. I., Bolton J. M., Fudenberg H. H. Haptoglobins, transferrins and serum gamma-globulin types in Malayan aborigines. Nature. 1967 Aug 12;215(5102):777–777. doi: 10.1038/215777a0. [DOI] [PubMed] [Google Scholar]
  4. Fessas P., Eng L. I., Na-Nakorn S., Todd D., Clegg J. B., Weatherall D. J. Identification of slow-moving haemoglobins in haemoglobin H disease from different racial groups. Lancet. 1972 Jun 17;1(7764):1308–1310. doi: 10.1016/s0140-6736(72)91036-7. [DOI] [PubMed] [Google Scholar]
  5. HAUT A., TUDHOPE G. R., CARTWRIGHT G. E., WINTROBEMM The nonhemoglobin erythrocytic proteins, studied by electrophoresis on starch gel. J Clin Invest. 1962 Mar;41:579–587. doi: 10.1172/JCI104512. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. LIE-INJOLUAN E. N. G., CHIN J. ABNORMAL HAEMOGLOBIN AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN MALAYAN ABORIGINES. Nature. 1964 Oct 17;204:291–292. doi: 10.1038/204291a0. [DOI] [PubMed] [Google Scholar]
  7. Lie-Injo L. E., Fix A., Bolton J. M., Gilman R. H. Haemoglobin E-hereditary elliptocytosis in Malayan aborigines. Acta Haematol. 1972;47(4):210–216. doi: 10.1159/000208526. [DOI] [PubMed] [Google Scholar]
  8. Lie-Injo L. E. Haemoglobin Bart's and slow-moving haemoglobin x components in newborns. The homozygous state for the slow-moving X components in a Malay boy. Acta Haematol. 1973;49(1):25–35. doi: 10.1159/000208382. [DOI] [PubMed] [Google Scholar]
  9. Lie-Injo L. E., Lopez C. G., Lopes M. Inheritance of haemoglobin H disease. A new aspect. Acta Haematol. 1971;46(2):106–120. doi: 10.1159/000208565. [DOI] [PubMed] [Google Scholar]
  10. Milner P. F., Clegg J. B., Weatherall D. J. Haemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain. Lancet. 1971 Apr 10;1(7702):729–732. doi: 10.1016/s0140-6736(71)91992-1. [DOI] [PubMed] [Google Scholar]
  11. Scott R. B. Rapid technic for preparation of hemoglobin solutions for electrophoresis. Am J Clin Pathol. 1970 Jul;54(1):78–81. doi: 10.1093/ajcp/54.1.78. [DOI] [PubMed] [Google Scholar]
  12. Todd D. Slow-moving haemoglobin bands in haemoglobin-H disease. Lancet. 1971 Aug 21;2(7721):439–439. doi: 10.1016/s0140-6736(71)90157-7. [DOI] [PubMed] [Google Scholar]
  13. Wasi P., Na-Nakorn S., Pootrakul P., Panich V. Incidence of haemoglobin Thai: a re-examination of the genetics of alpha-thalassaemic diseases. Ann Hum Genet. 1972 Apr;35(4):467–470. doi: 10.1111/j.1469-1809.1957.tb01871.x. [DOI] [PubMed] [Google Scholar]
  14. Wasi P., Na-Nakorn S., Pootrakul S., Sookanek M., Disthasongchan P., Panich V., Pornpatkul M. Alpha- and beta-thalassemia in Thailand. Ann N Y Acad Sci. 1969 Nov 20;165(1):60–82. doi: 10.1111/j.1749-6632.1969.tb27777.x. [DOI] [PubMed] [Google Scholar]

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