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Correlations with Point Mutations and Severity of Hemolitic Anemias: The Example of Hereditary Persistence of Fetal Hemoglobin with Sickle Cell Anemia and Beta Thalassemia

By Anderson Ferreira da Cunha, Iran Malavazi, Karen Simone Romanello and Cintia do Couto Mascarenhas

Submitted: May 20th 2011Reviewed: January 11th 2012Published: March 21st 2012

DOI: 10.5772/36240

Downloaded: 1815

© 2012 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Anderson Ferreira da Cunha, Iran Malavazi, Karen Simone Romanello and Cintia do Couto Mascarenhas (March 21st 2012). Correlations with Point Mutations and Severity of Hemolitic Anemias: The Example of Hereditary Persistence of Fetal Hemoglobin with Sickle Cell Anemia and Beta Thalassemia, Point Mutation Colin Logie, IntechOpen, DOI: 10.5772/36240. Available from:

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