Detection and identification of β-thalassemia 3.5 kb deletion by SYBR Green1 and high resolution melting analysis
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2008.01173.x/fullpdf
Reference8 articles.
1. Molecular characterization of a high A2 beta thalassemia by direct sequencing of single strand enriched amplified genomic DNA;Thein;Blood,1989
2. Molecular characterization of a novel 10.3 kb deletion causing beta-thalassaemia with unusually high Hb A2;Craig;Br J Haematol,1992
3. A novel 105 basepair deletion causing beta(0)-thalassemia in members of a Thai family;Nopparatana;Am J Hematol,1999
4. Characterization of the breakpoint of a 3.5-kb deletion of the beta-globin gene;Lynch;Genomics,1991
5. Beta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin gene;Sanguansermsri;Hemoglobin,1990
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4. High-resolution melting analysis for prenatal diagnosis of beta-thalassemia in northern Thailand;International Journal of Hematology;2017-08-08
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