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Frequency of hemoglobin E/β-thalassemia compound heterozygotes with low hemoglobin F phenotype among cases with a diagnosis of hemoglobin E homozygote, determined by high-performance liquid chromatography, in prenatal control program for β-thalassemia.
Wong P, Srichaiya A, Suannum P, Charoenporn P, Jermnim S, Chan-In M, Tapprom A, Deoisares R. Wong P, et al. Among authors: tapprom a. Ann Hematol. 2017 Oct;96(10):1763-1765. doi: 10.1007/s00277-017-3089-4. Epub 2017 Aug 12. Ann Hematol. 2017. PMID: 28803407 No abstract available.
Essential genetic modifiers and their measurable impact in a community-recruited population analysis for non-severe hemoglobin E/β-thalassemia prenatal genetic counseling.
Wong P, Chitsobhak T, Jittasathian S, Sirichantharawat C, Cherdchoo N, Prangcharoen W, Jongautchariyakul P, Jampachaisri K, Tapprom A, Deoisares R, Chumnumsiriwath P. Wong P, et al. Among authors: tapprom a. Blood Cells Mol Dis. 2023 Nov;103:102765. doi: 10.1016/j.bcmd.2023.102765. Epub 2023 Jun 15. Blood Cells Mol Dis. 2023. PMID: 37353362