Severe thalassaemia intermedia caused by interaction of homozygosity for α-globin gene triplication with heterozygosity for β thalassaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1994.tb04743.x/fullpdf
Reference11 articles.
1. Identification of deletion and triple α-globin gene haplotypes in the montreal β-thalassemia screening program: Implications for genetic medicine
2. A benign form of thalassaemia intermedia may be determined by the interaction of triplicated α locus and heterozygous β-thalassaemia
3. A family with segregating triplicated alpha globin loci and beta thalassemia
4. FREQUENCIES OF COMMON β-THALASSAEMIA ALLELES AMONG DIFFERENT POPULATIONS: VARIABILITY IN CLINICAL SEVERITY
5. The triplicated α gene locus and β thalassaemia
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1. Beta‐thalassemia intermedia due to a complex alpha‐globin rearrangement and a heterozygous beta thalassemia mutation;British Journal of Haematology;2024-08-18
2. Support Vector Machine-Based Formula for Detecting Suspected α Thalassemia Carriers: A Path toward Universal Screening;International Journal of Molecular Sciences;2024-06-11
3. Impact of α-Globin Gene Expression and α-Globin Modifiers on the Phenotype of β-Thalassemia and Other Hemoglobinopathies: Implications for Patient Management;International Journal of Molecular Sciences;2024-03-17
4. Transfusion requirements and complication rate in β‐thalassemia intermedia due to heterozygous β‐globin gene mutation and triplicated α‐globin genes;European Journal of Haematology;2023-07-30
5. The hemoglobinopathies, molecular disease mechanisms and diagnostics;International Journal of Laboratory Hematology;2022-09
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