Characterization of β-thalassemia mutations by denaturing gradient gel electrophoresis: patterns in the Mediterranean mutations
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1994.tb04145.x/fullpdf
Reference11 articles.
1. Rapid prenatal diagnosis of β-thalassemia using DNA amplification and nonradioactive probes;Cai;Blood,1989
2. Identification of multiple β-thalassemia mutations by denaturing gradient gel electrophoresis;Cai;J Clin Invest,1990
3. Simultaneous screening for β-thalassemia mutations by chemical cleavage of mismatch;Dianzani;Genomics,1991
4. Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean β-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in Sicily;Maggio;Blood,1993
5. Detection of single base substitution by ribonuclease cleavage at mismatches in RNA:DNA duplexes;Myers;Science,1988
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