https://orcid.org/0000-0003-4111-7910
References
- Weatherall DJ, Clegg JB. The Thalassaemia Syndromes, 4 ed. Oxford (Oxfordshire, UK): Blackwell Science; 2001.
- Silva AN, Cardoso GL, Cunha DA, et al. The spectrum of β-thalassemia mutations in a population from the Brazilian Amazon. Hemoglobin. 2016;40(1):20–24.
- Yamsri S, Sanchaisuriya K, Fucharoen G, et al. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand. Blood Cells Mol Dis. 2011;47(2):120–124.
- Viprakasit V, Limwongse C, Sukpanichnant S, et al. Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from Thailand. Clin Chem Lab Med. 2013;51(8):1605–1614.
- Nopparatana C, Nopparatana C, Saechan V, et al. Prenatal diagnosis of α- and β-thalassemias in southern Thailand. Int J Hematol. 2020;111(2):284–292.
- Fucharoen G, Srivorakun H, Singsanan S, et al. Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system. Int J Lab Hematol. 2011;33(4):424–433.
- Yamsri S, Sanchaisuriya K, Fucharoen G, et al. Prevention of severe thalassemia in northeast Thailand: 16 years of experience at a single university center. Prenat Diagn. 2010;30(6):540–546.
- Tepakhan W, Jomoui W. Rapid molecular detection for differentiation of homozygous Hb E and β0-thalassemia/Hb E in samples related with Hb E >80% and variable Hb F levels. Lab Med. 2020;2020;lmaa065.
- Sirichotiyakul S, Saetung R, Sanguansermsri T. Analysis of β-thalassemia mutations in northern Thailand using an automated fluorescence DNA sequencing technique. Hemoglobin. 2003;27(2):89–95.
- Jomoui W, Tepakhan W. Characterization and identification of Prachinburi β0-thalassemia: a novel-60 kb deletion in β globin gene related to high levels of Hb F in heterozygous state. Int J Lab Hematol. 2021. DOI:10.1111/ijlh.13511
- Tepakhan W, Srewaradachpisal K, Kanjanaopas S, et al. Genetics background of β-thalassemia (3.5 kb deletion) in Southern Thailand: haplotype analysis using novel reverse dot blot hybridization. Ann Hum Genet. 2021;85(3–4):115–124. Epub 2021 Feb 8.
- Chaweephisal P, Phusua A, Fanhchaksai K, et al. Borderline hemoglobin A2 levels in northern Thai population: HBB genotypes and effects of coinherited alpha-thalassemia. Blood Cells Mol Dis. 2019;74:13–17.
- Charoenporn P, Wong P, Mirasena S, et al. The spectrum of β thalassemia mutations in Phitsanulok. J Hematol Transfus Med. 2013;23(4):277–282.
- Perseu L, Satta S, Moi P, et al. KLF1 gene mutations cause borderline HbA(2)). Blood. 2011;118(16):4454–4458.
- De Angioletti M, Sabato V, Musollino G, et al. South-Italy β0-thalassemia: a novel deletion not removing the γ-globin silencing element and with 3′ breakpoint in a hsRTVL-H element, associated with β0-thalassemia and high levels of Hb F. Haematologica. 2013;98(8):e98–e100.
- Yamsri S, Singha K, Prajantasen T, et al. A large cohort of β(+)-thalassemia in Thailand: molecular, hematological and diagnostic considerations. Blood Cells Mol Dis. 2015;54(2):164–169.