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Journal Abstract Search

226 related items for PubMed ID: 11522274

  • 1. Simultaneous PCR detection of beta - thalassemia and alpha - thalassemia 1 (SEA type) in prenatal diagnosis of complex thalassemia syndrome.
    Siriratmanawong N, Fucharoen G, Sanchaisuriya K, Ratanasiri T, Fucharoen S.
    Clin Biochem; 2001 Jul; 34(5):377-80. PubMed ID: 11522274
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  • 2. [Genetic diagnosis of alpha and beta thalassemia dual heterozygote].
    Zeng R, Yu S, Hu B.
    Zhonghua Xue Ye Xue Za Zhi; 1998 Oct; 19(10):525-7. PubMed ID: 11189497
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  • 4. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N, Pinmuang-Ngam C, Fucharoen G, Fucharoen S.
    Fetal Diagn Ther; 2007 Oct; 22(4):264-8. PubMed ID: 17369692
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  • 5. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.
    Li D, Liao C, Li J, Xie X, Huang Y, Zhong H.
    Haematologica; 2006 May; 91(5):649-51. PubMed ID: 16627247
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  • 6. Prenatal diagnosis based on simultaneous DNA analysis for alpha- and beta-globin genes.
    Oron-Karni V, Filon D, Rund D, Rachmilewitz E, Oppenheim A.
    Am J Hematol; 1996 Nov; 53(3):203-4. PubMed ID: 8895695
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  • 7. 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; 83(1):57-65. PubMed ID: 19226360
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  • 8. [Large-scale population-based genetic screening and prenatal diagnosis for thalassemias in Zhuhai City of Guangdong Province].
    Zhou YQ, Shang X, Yin BM, Xiong F, Xiao QZ, Zhou WJ, Zhang YL, Xu XM.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):90-5. PubMed ID: 22455738
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  • 11. Alpha and beta thalassemias in Hong Kong.
    Chan V, Chan TK, Todd D.
    Chin Med J (Engl); 1997 Jun; 110(6):490-3. PubMed ID: 9594254
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  • 12. Genetic origin and interaction of the Filipino β⁰-thalassemia with Hb E and α-thalassemia in a Thai family.
    Yamsri S, Sanchaisuriya K, Fucharoen G, Fucharoen S.
    Transl Res; 2012 Jun; 159(6):473-6. PubMed ID: 22633098
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  • 14. [Genetic diagnosis of thalassemia mutations with free fetal DNA in pregnant plasma].
    Lin XR, You LX, Chen Y.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2013 Oct; 21(5):1215-9. PubMed ID: 24156437
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  • 15. 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
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  • 19. Prenatal diagnosis of a case with SEA-HPFH deletion thalassemia with whole HBB gene deletion.
    Ly Thi Thanh H, Le Thi Thanh H, Hoang Luong L, Huy Tran T, Liu SC, Truong HN, Ta TV, Bui TH, Tran VK.
    Taiwan J Obstet Gynecol; 2018 Jun 15; 57(3):435-441. PubMed ID: 29880180
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