Characterization and identification of Prachinburi β 0 ‐thalassemia: A novel‐60 kb deletion in beta globin gene related to high levels of Hb F in heterozygous state
Author:
Affiliation:
1. Department of Pathology Maha Chakri Sirindhorn Medical Center Faculty of Medicine Srinakharinwirot University Nakhon Nayok Thailand
2. Department of Pathology Faculty of Medicine Prince of Songkla University Songkhla Thailand
Publisher
Wiley
Subject
Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijlh.13511
Reference12 articles.
1. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand
2. A novel 223 kb deletion in the beta‐globin gene cluster was identified in a Chinese thalassemia major patient
3. Characterization of a Novel Deletion Causing β-Thalassemia Major in an Afghan Family
4. Variability of hemoglobin F expression in hemoglobin EE disease: Hematological and molecular analysis
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1. Targeted Next-Generation Sequencing Reveals a Large Novel β-Thalassemia Deletion that Removes the Entire HBB Gene;Hemoglobin;2022-09-03
2. Molecular Epidemiology and Hematologic Characterization of Thalassemia in Guangdong Province, Southern China;Clinical and Applied Thrombosis/Hemostasis;2022-01
3. Rapid molecular diagnostics of large deletional β0-thalassemia (3.5 kb and 45 kb) using colorimetric LAMP in various thalassemia genotypes;Heliyon;2021-11
4. Molecular Spectrum of β-Thalassemia Mutations in Central to Eastern Thailand;Hemoglobin;2021-05-10
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