The detection of β-globin gene mutations in β-thalassemia using oligonucleotide probes and amplified DNA
Author:
Publisher
Elsevier BV
Subject
Genetics,Biochemistry,Biophysics,Structural Biology
Reference18 articles.
1. Hemoglobin: Molecular, Genetic and Clinical Aspects;Bunn,1986
2. The Thalassemia Repository
3. A β-thalassemia ledon abolishes the sameMstII site as the sickle mutation
4. Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster
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1. Efficient Detection of Mediterranean β-Thalassemia Mutations by Multiplex Single-Nucleotide Primer Extension;PLoS ONE;2012-10-26
2. Comprehensive and EfficientHBBMutation Analysis for Detection of β-Hemoglobinopathies in a Pan-Ethnic Population;American Journal of Clinical Pathology;2010-05
3. Molecular Basis of β-Thalassemia and Other Hemoglobinopathies in Bulgaria: An Update;Hemoglobin;2007-01
4. Multiplex Minisequencing Screen for Common Southeast Asian and Indian β-Thalassemia Mutations;Clinical Chemistry;2003-02-01
5. Spectrum of ?-thalassemia in Jordan: Identification of two novel mutations;American Journal of Hematology;2001
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