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Issue Date
Title
Author(s)
2021
Genetics background of β-thalassemia (3.5 kb deletion) in Southern Thailand: Haplotype analysis using novel reverse dot blot hybridization
Tepakhan W.
;
Srewaradachpisal K.
;
Kanjanaopas S.
;
Jomoui W.
2020
Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand
Jomoui W.
;
Tepakhan W.
;
Satthakarn S.
;
Panyasai S.
2021
Molecular Spectrum of β-Thalassemia Mutations in Central to Eastern Thailand
Panichchob P.
;
Iamdeelert P.
;
Wongsariya P.
;
Wongsariya P.
;
Wongwattanasanti P.
;
Tepakhan W.
;
Jomoui W.
2019
Coinheritance 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 Tube
Jomoui W.
;
Panichchob P.
;
Rujirachaivej P.
;
Panyasai S.
;
Tepakhan W.
2021
Characterization and identification of Prachinburi β0-thalassemia: A novel-60 kb deletion in beta globin gene related to high levels of Hb F in heterozygous state
Jomoui W.
;
Tepakhan W.
2017
Molecular analysis of haemoglobin E in Southeast Asian populations
Jomoui W.
;
Fucharoen G.
;
Sanchaisuriya K.
;
Nguyen N.T.
;
Nguyen H.V.
;
Fucharoen S.
2020
A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders
Jomoui W.
;
Tepakhan W.
;
Yamsri S.
;
Srivorakun H.
;
Fucharoen G.
;
Fucharoen S.
2019
Strong 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 Thailand
Jomoui W.
;
Tepakhan W.
;
Karnpean R.
2022
Genetic Background Studies of Eight Common Beta Thalassemia Mutations in Thailand Using β-Globin Gene Haplotype and Phylogenetic Analysis
Karnpean R.
;
Tepakhan W.
;
Suankul P.
;
Thingphom S.
;
Poonsawat A.
;
Thanunchaikunlanun N.
;
Ruangsanngamsiri R.
;
Jomoui W.
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1
Iamdeelert P.
1
Kanjanaopas S.
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Nguyen H.V.
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