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757 related items for PubMed ID: 21664157

  • 1. Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand.
    Yamsri S, Sanchaisuriya K, Fucharoen G, Sae-Ung N, Fucharoen S.
    Blood Cells Mol Dis; 2011 Aug 15; 47(2):120-4. PubMed ID: 21664157
    [Abstract] [Full Text] [Related]

  • 2. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS, He J, Zhang J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb 15; 47(2):85-9. PubMed ID: 22455737
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  • 3. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.
    Prakobkaew N, Fucharoen S, Fuchareon G, Siriratmanawong N.
    Eur J Haematol; 2014 Jan 15; 92(1):73-9. PubMed ID: 24112054
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  • 4. Molecular and hematologic features of hemoglobin E heterozygotes with different forms of alpha-thalassemia in Thailand.
    Sanchaisuriya K, Fucharoen G, Sae-ung N, Jetsrisuparb A, Fucharoen S.
    Ann Hematol; 2003 Oct 15; 82(10):612-6. PubMed ID: 12955472
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  • 5. High frequency of deletional alpha-thalassemia in beta-thalassemia trait: implications for genetic counseling.
    Panigrahi I, Rafeeq PH, Choudhry VP, Saxena R.
    Am J Hematol; 2004 Jul 15; 76(3):297-9. PubMed ID: 15224373
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  • 6. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
    Panyasai S, Fucharoen S, Surapot S, Fucharoen G, Sanchaisuriya K.
    Haematologica; 2004 Jul 15; 89(7):777-81. PubMed ID: 15257928
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  • 8. A large cohort of β(+)-thalassemia in Thailand: molecular, hematological and diagnostic considerations.
    Yamsri S, Singha K, Prajantasen T, Taweenan W, Fucharoen G, Sanchaisuriya K, Fucharoen S.
    Blood Cells Mol Dis; 2015 Feb 15; 54(2):164-9. PubMed ID: 25471338
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  • 10. Silent thalassemias: genotypes and phenotypes.
    Bianco I, Cappabianca MP, Foglietta E, Lerone M, Deidda G, Morlupi L, Grisanti P, Ponzini D, Rinaldi S, Graziani B.
    Haematologica; 1997 Feb 15; 82(3):269-80. PubMed ID: 9234571
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  • 11. [A community-based genetic screening of large-scale population and prenatal diagnosis for alpha and beta thalassemia in Zhuhai city of Guangdong province].
    Zhou YQ, Mo QH, Lu JH, Li LY, Liang X, Jia SQ, Xiao GF, Zhou WJ, Xiao QZ, Xu XM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Jun 15; 25(3):256-61. PubMed ID: 18543211
    [Abstract] [Full Text] [Related]

  • 12. Co-inheritance of alpha-and beta-thalassemia in Khuzestan Province, Iran.
    Rahim F, Kaikhaei B, Zandian K, Hoseini A.
    Hematology; 2008 Feb 15; 13(1):59-64. PubMed ID: 18534068
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  • 13. Prevalence and genetic analysis of α-thalassemia and β-thalassemia in Chongqing area of China.
    Yao XY, Yu J, Chen SP, Xiao JW, Zheng QC, Liu HY, Zhang L, Xian Y, Zou L.
    Gene; 2013 Dec 10; 532(1):120-4. PubMed ID: 24055728
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  • 15. [Genetic diagnosis of alpha and beta thalassemia dual heterozygote].
    Zeng R, Yu S, Hu B.
    Zhonghua Xue Ye Xue Za Zhi; 1998 Oct 10; 19(10):525-7. PubMed ID: 11189497
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  • 18. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
    Srivorakun H, Fucharoen G, Sae-Ung N, Sanchaisuriya K, Ratanasiri T, Fucharoen S.
    Eur J Haematol; 2009 Jul 10; 83(1):57-65. PubMed ID: 19226360
    [Abstract] [Full Text] [Related]

  • 19. Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A2 Levels.
    Satthakarn S, Panyasai S, Pornprasert S.
    Hemoglobin; 2020 Sep 10; 44(5):349-353. PubMed ID: 33023363
    [Abstract] [Full Text] [Related]

  • 20. Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand.
    Panyasai S, Pornprasert S.
    Hemoglobin; 2020 May 10; 44(3):179-183. PubMed ID: 32482156
    [Abstract] [Full Text] [Related]

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