Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes
Author:
Publisher
Informa UK Limited
Subject
Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1586/17474086.2015.1075385
Reference23 articles.
1. Elucidating the spectrum of -thalassemia mutations in Iran
2. High Prevalence of the −α3.7Deletion Among Thalassemia Patients in Iran
3. Frequency of α-Globin Gene Triplications and Their Interaction with β-Thalassemia Mutations
4. Interaction of anα-Globin Gene Triplication withβ-Globin Gene Mutations in Iranian Patients withβ-Thalassemia Intermedia
5. Segmental duplications involving the α-globin gene cluster are causing β-thalassemia intermedia phenotypes in β-thalassemia heterozygous patients
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2. Production and Characterization of K562 Cellular Clones Hyper-Expressing the Gene Encoding α-Globin: Preliminary Analysis of Biomarkers Associated with Autophagy;Genes;2023-02-23
3. Co-inherited α-Globin Gene Cluster Duplication Compromises RBC Indices-Based Thalassemia Screening;Indian Journal of Hematology and Blood Transfusion;2022-11-04
4. The hemoglobinopathies, molecular disease mechanisms and diagnostics;International Journal of Laboratory Hematology;2022-09
5. Third-generation sequencing: A novel tool detects complex variants in the α-thalassemia gene;Gene;2022-05
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