SYTO9 and SYBR GREEN1 with a high-resolution melting analysis for prenatal diagnosis of β0-thalassemia/hemoglobin-E
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2010.01512.x/fullpdf
Reference21 articles.
1. SYTO9 and SYBR GREEN1 with high resolution melting analysis for molecular confirmatory testing of the common Southeast Asian beta(0)-thalassemia mutations;Chamras;Hemoglobin,2009
2. Detection of beta-thalassemia mutations using a multiplex amplification refractory mutation system assay;Mirasena;Hemoglobin,2008
3. Thalassemia in SouthEast Asia: problems and strategy for prevention and control;Fucharoen;Southeast Asian J Trop Med Public Health,1992
4. Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine;Fucharoen;Hemoglobin,1997
5. Defective synthesis of HbE is due to reduced levels of beta E mRNA;Traeger;Nature,1980
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1. Multiplex Quantitative Real-Time Polymerase Chain Reaction and High-Resolution Melting Analysis for Identification of a Couple At-Risk of Having a Newborn with Severe Thalassemia;Hemoglobin;2021-09-03
2. Analysis of theXmn1-Gγ polymorphism in β-thalassemia/hemoglobin E (HbE) and homozygous HbE patients with low and high levels of HbF;International Journal of Laboratory Hematology;2014-07-08
3. Detection of β-Thalassemia/Hemoglobin E Disease in Samples which Initially were Diagnosed as Homozygous Hemoglobin E;Clinical Laboratory;2013
4. Rapid Identification of Heterozygous and Homozygous Hemoglobin Constant Spring by SYTO9 with a High Resolution Melting Analysis;Clinical Laboratory;2013
5. Coinheritance of Hb S [β6(A3)Glu→Val, GAG>GTG] with β0-Thalassemia Codon 17 (A>T) in a Thai Patient;Hemoglobin;2012-04-03
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