Determination of the breakpoint and molecular diagnosis of a common α-thalassaemia-1 deletion in the Indian population
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-141.2003.04704.x/fullpdf
Reference15 articles.
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2. Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, India;Fodde;Human Genetics,1988
3. Multiple recombination events are responsible for the heterogeneity of alpha(+)-thalassemia haplotypes among the forest tribes of Andhra Pradesh, India;Fodde;Annals of Human Genetics,1991
4. HbH disease in Sardinia: molecular, hematological and clinical aspects;Galanello;Acta Haematologica,1992
5. Rapid detection of point mutations and polymorphisms of the alpha-globin genes by DGGE and SSCA;Harteveld;Human Mutation,1996
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