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. 1987 Oct;24(10):578–583. doi: 10.1136/jmg.24.10.578

Disorders of haemoglobin in China.

Y T Zeng 1, S Z Huang 1
PMCID: PMC1050282  PMID: 3500312

Abstract

A large scale survey of haemoglobinopathies and thalassaemia has been carried out in China, involving 900,000 people in 28 provinces. It has resulted in the finding of many new variants and some interesting cases of thalassaemia, and in a study on the chemical structure of abnormal haemoglobins and DNA analysis of thalassaemia. We report here data on haemoglobin disorders in the Chinese, mainly the characterisation of the geographical distribution of haemoglobin variants, the analysis of globin genes of alpha, beta, gamma, or delta beta thalassaemia, and the progress in prenatal diagnosis of alpha and beta thalassaemia conducted in the authors' laboratory.

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Selected References

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

  1. Antonarakis S. E., Kazazian H. H., Jr, Orkin S. H. DNA polymorphism and molecular pathology of the human globin gene clusters. Hum Genet. 1985;69(1):1–14. doi: 10.1007/BF00295521. [DOI] [PubMed] [Google Scholar]
  2. Cheng T. C., Orkin S. H., Antonarakis S. E., Potter M. J., Sexton J. P., Markham A. F., Giardina P. J., Li A., Kazazian H. H., Jr beta-Thalassemia in Chinese: use of in vivo RNA analysis and oligonucleotide hybridization in systematic characterization of molecular defects. Proc Natl Acad Sci U S A. 1984 May;81(9):2821–2825. doi: 10.1073/pnas.81.9.2821. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Orkin S. H., Kazazian H. H., Jr, Antonarakis S. E., Goff S. C., Boehm C. D., Sexton J. P., Waber P. G., Giardina P. J. Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster. Nature. 1982 Apr 15;296(5858):627–631. doi: 10.1038/296627a0. [DOI] [PubMed] [Google Scholar]
  4. Zeng Y. T., Huang S. Z. Alpha-globin gene organisation and prenatal diagnosis of alpha-thalassaemia in Chinese. Lancet. 1985 Feb 9;1(8424):304–307. doi: 10.1016/s0140-6736(85)91081-5. [DOI] [PubMed] [Google Scholar]
  5. Zeng Y. T., Huang S. Z., Chen B., Liang Y. C., Chang Z. M., Harano T., Huisman T. H. Hereditary persistence of fetal hemoglobin or (delta beta)o-thalassemia: three types observed in South-Chinese families. Blood. 1985 Dec;66(6):1430–1435. [PubMed] [Google Scholar]
  6. Zeng Y. T., Huang S. Z., Nakatsuji T., Huisman T. H. -G gamma A gamma-Thalassemia and gamma-chain variants in Chinese newborn babies. Am J Hematol. 1985 Mar;18(3):235–242. doi: 10.1002/ajh.2830180303. [DOI] [PubMed] [Google Scholar]

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