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Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 4
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Original Article

A Simple Approach to the Characterization of Three Common Indian β-Thalassemia Mutations by Artificially Created Restriction Sites

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Pages 311-318 | Received 24 Feb 2000, Accepted 14 May 2000, Published online: 07 Jul 2009

References

  • Gorakshakar A. C., Pawar A. R., Nadkarni A. H., Lu C. Y., Mohanty D., Krishnamoorthy R., Besmond C., Colah R. B. Potential of denaturing gradient gel electrophoresis for scanning of β‐thalassemia mutations in India. Am. J. Hematol. 1999; 61: 120–125
  • Kwok S., Kellogg D. E., Mc Kinney N., Spasic D., Goda L., Levenson C., Sninsky J. J. Effect of primer‐template mismatches on the polymerase chain reaction: human immunodeficiency virus type I model studies. Nucleic Acids Res. 1990; 18: 999–1005
  • Haliassos A., Chomel J. C., Tesson L., Baudis M., Kruh J., Kaplan J. C., Kitzis A. Modification of enzymatically amplified DNA for the detection of point mutation. Nucleic Acids Res. 1989; 17: 3606
  • Eiken H. G., Odland E., Boman H., Skjelkvale L., Engebretsen L. F., Apold J. Application of natural and amplification created restriction sites for the diagnosis of PKU mutations. Nucleic Acids Res. 1991; 19: 1427–1430
  • Sorscher E. J., Huang Z. Diagnosis of genetic disease by primer‐specified restriction map modification with application to cystic fibrosis and retinitis pigmentosa. The Lancet 1991; 337: 1115–1118
  • Lindeman R., Hu S. P., Volpato F., Trent R. J. Polymerase chain reaction (PCR) mutagenesis enabling rapid non‐radioactive detection of common β‐thalassemia mutations in Mediterraneans. Br. J. Haematol. 1991; 78: 100–104
  • Chang J. G., Chen P. H., Chiou S. S., Lee L. S., Perng L. I., Liu T. C. Rapid diagnosis of β‐thalassemia mutations in Chinese by naturally and amplified created restriction sites. Blood 1992; 80: 2092–2096
  • Varawalla N. Y., Old J. M., Sarkar R., Venkatesan R., Weatherall D. J. The spectrum of β‐thalassemia mutations on the Indian subcontinent: the basis for prenatal diagnosis. Br. J. Haeniatol. 1991; 78: 242–247
  • Liu T. C., Lin S. F., Yang T. Y., Lee J. P., Chen T. P., Chang J. G. Prenatal diagnosis of thalassemia in the Chinese. Am. J. Hematol. 1997; 55: 65–68

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