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Lessons learned from a prenatal diagnosis program for thalassemia in Thailand.
Prenat Diagn. 2020 Jul;40(8):998-1004. doi: 10.1002/pd.5723. Epub 2020 May 13.
Prenat Diagn. 2020.
PMID: 32356374
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: charoenporn p.
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.
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A blood transfusion leading to misdiagnosis of beta-thalassaemia carrier status.
Wong P, Tapprom A, Jermnim N, Charoenporn P, Kanthiyawong S.
Wong P, et al. Among authors: charoenporn p.
Blood Transfus. 2010 Jan;8(1):69-70. doi: 10.2450/2009.0087-09.
Blood Transfus. 2010.
PMID: 20104282
Free PMC article.
No abstract available.
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Rapid diagnosis of alpha(o)-thalassemia using the relative quantitative PCR and the dissociation curve analysis.
Sangkitporn SK, Wangkahat K, Sangnoi A, Songkharm B, Charoenporn P, Sangkitporn S.
Sangkitporn SK, et al. Among authors: charoenporn p.
Clin Lab Haematol. 2003 Dec;25(6):359-65. doi: 10.1046/j.0141-9854.2003.00549.x.
Clin Lab Haematol. 2003.
PMID: 14641139
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