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Issue DateTitleAuthor(s)
2021Genetics background of β-thalassemia (3.5 kb deletion) in Southern Thailand: Haplotype analysis using novel reverse dot blot hybridizationTepakhan W.; Srewaradachpisal K.; Kanjanaopas S.; Jomoui W.
2020Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in ThailandJomoui W.; Tepakhan W.; Satthakarn S.; Panyasai S.
2021Molecular Spectrum of β-Thalassemia Mutations in Central to Eastern ThailandPanichchob P.; Iamdeelert P.; Wongsariya P.; Wongsariya P.; Wongwattanasanti P.; Tepakhan W.; Jomoui W.
2019Coinheritance of Hb A2-Melbourne (HBD: c.130G>A) and Hb E (HBB: c.79G>A) in Laos and Simultaneous High Resolution Melt Detection of Hb A2-Melbourne and Hb A2-Lampang (HBD: c.142G>A) in a Single TubeJomoui W.; Panichchob P.; Rujirachaivej P.; Panyasai S.; Tepakhan W.
2021Characterization and identification of Prachinburi β0-thalassemia: A novel-60 kb deletion in beta globin gene related to high levels of Hb F in heterozygous stateJomoui W.; Tepakhan W.
2017Molecular analysis of haemoglobin E in Southeast Asian populationsJomoui W.; Fucharoen G.; Sanchaisuriya K.; Nguyen N.T.; Nguyen H.V.; Fucharoen S.
2020A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disordersJomoui W.; Tepakhan W.; Yamsri S.; Srivorakun H.; Fucharoen G.; Fucharoen S.
2019Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (– –SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart’s Hydrops Fetalis Syndrome in ThailandJomoui W.; Tepakhan W.; Karnpean R.

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