HbA2 levels in β-thalassaemia carriers with the Filipino β0-deletion: are the levels higher than what is found with non-deletional forms of β0-thalassaemia?
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference36 articles.
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3. The spectrum of beta-globin gene mutations in children with beta-thalassaemia major from Kota-Kinabalu, Sabah, Malaysia;Thong;Singapore Med J,2005
4. Filipino b0 thalassaemia: a high Hb A2 b0 thalassaemia resulting from a large deletion of the 50 b globin gene region;Motum;J Med Genet,1993
5. Identification of two novel b zero-thalassemia mutations in a Filipino family: frameshift codon 67 (-TG) and a β-globin gene deletion;Eng;Hum Mutat,1993
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1. First Report of Filipino β 0 -Thalassemia/β-Thalassemia in a Chinese Family;Hemoglobin;2024-01-02
2. Characterization of β-Globin Gene Cluster Deletions Using Multiplex-Gap Polymerase Chain Reaction (PCR) and Multiplex Ligation-Dependent Probe Amplification (MLPA);Bangladesh Journal of Medical Science;2021-04-04
3. Application of HbA 2 levels and red cell indices‐based new model in the differentiation of thalassemia traits from iron deficiency in hypochromic microcytic anemia Cases;International Journal of Laboratory Hematology;2020-06-21
4. Borderline hemoglobin A2 levels in northern Thai population: HBB genotypes and effects of coinherited alpha-thalassemia;Blood Cells, Molecules, and Diseases;2019-02
5. Haplotype Analysis of β-Thalassaemia Major and Carriers with Filipino β°-Deletion in Sabah, Malaysia;Malaysian Journal of Medical Sciences;2018
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