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Showing results 6 to 14 of 14 < previous

Issue Date	Title	Author(s)
2022	Loop-mediated isothermal amplification (LAMP) colorimetric phenol red assay for rapid identification of α0-thalassemia: Application to population screening and prenatal diagnosis	Jomoui W.; Srivorakun H.; Chansai S.; Fucharoen S.
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	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.
2023	Molecular understanding of unusual HbE-β+-thalassemia with Hb phenotype similar to HbE heterozygote: simple and rapid differentiation using HbE levels	Jomoui W.; Satthakarn S.; Panyasai S.; Srinakharinwirot University
2021	Rapid Molecular Detection for Differentiation of Homozygous HbE and ß0-Thalassemia/HbE in Samples Related With HbE >80% and Variable HbF Levels	Tepakhan W.; Jomoui W.
2021	Rapid molecular diagnostics of large deletional β0-thalassemia (3.5 kb and 45 kb) using colorimetric LAMP in various thalassemia genotypes	Tepakhan W.; Jomoui W.
2023	Revisiting and updating molecular epidemiology of α-thalassemia mutations in Thailand using MLPA and new multiplex gap-PCR for nine α-thalassemia deletion	Jomoui W.; Panyasai S.; Sripornsawan P.; Tepakhan W.; Srinakharinwirot University
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.

Showing results 6 to 14 of 14 < previous