Diagnosis and prevention of thalassemia
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,General Biochemistry, Genetics and Molecular Biology
Link
http://www.tandfonline.com/doi/pdf/10.3109/10408363.2013.847236
Reference125 articles.
1. Global epidemiology of haemoglobin disorders and derived service indicators
2. Prevalence and Genotypes of α- and β-Thalassemia Carriers in Hong Kong — Implications for Population Screening
3. Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?
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2. Screening for thalassemia carriers among the Han population of childbearing age in Southwestern of China;Frontiers in Genetics;2024-04-10
3. Identification of a novel 10.3 kb deletion causing α0-thalassemia by third-generation sequencing: Pedigree analysis and genetic diagnosis;Clinical Biochemistry;2023-03
4. NGS4THAL, a One-Stop Molecular Diagnosis and Carrier Screening Tool for Thalassemia and Other Hemoglobinopathies by Next-Generation Sequencing;The Journal of Molecular Diagnostics;2022-10
5. Prevalence and molecular characterization of common thalassemia among people of reproductive age in the border area of Guangxi-Yunnan-Guizhou province in Southwestern China;Hematology;2022-06-06
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