α-Globin Gene Quadruplication and Heterozygous β-Thalassemia: A Not So Rare Cause of Thalassemia Intermedia
Author:
Publisher
S. Karger AG
Subject
Hematology,General Medicine
Reference8 articles.
1. Association of globin gene quadruplication and heterozygous thalassemia in patients with thalassemia intermedia
2. MLPA and MAPH: New techniques for detection of gene deletions
3. Segmental duplications involving the α-globin gene cluster are causing β-thalassemia intermedia phenotypes in β-thalassemia heterozygous patients
4. Frequency of α-Globin Gene Triplications and Their Interaction with β-Thalassemia Mutations
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1. Co-inherited α-Globin Gene Cluster Duplication Compromises RBC Indices-Based Thalassemia Screening;Indian Journal of Hematology and Blood Transfusion;2022-11-04
2. The hemoglobinopathies, molecular disease mechanisms and diagnostics;International Journal of Laboratory Hematology;2022-09
3. Homeobox A5 and A9 expression and beta-thalassemia;British Journal of Biomedical Science;2021-03-12
4. α, β, δ and γ thalassaemias and related conditions;Haemoglobinopathy Diagnosis;2020-02-28
5. Three Mexican Families with β thalassemia intermedia with different molecular basis;Genetics and Molecular Biology;2019
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