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Journal Abstract Search

138 related items for PubMed ID: 17146943

  • 21. Identification of one or two α-globin gene deletions by isoelectric focusing electrophoresis.
    Agarwal AM, Nussenzveig RH, Hoke C, Lorey TS, Greene DN.
    Am J Clin Pathol; 2013 Sep; 140(3):301-5. PubMed ID: 23955447
    [Abstract] [Full Text] [Related]

  • 22. alpha-thalassemia mutations in Khuzestan Province, Southwest Iran.
    Zandian K, Nateghi J, Keikhaie B, Pedram M, Hafezi-Nejad N, Hadavi V, Oberkanins C, Azarkeivan A, Law HY, Najmabadi H.
    Hemoglobin; 2008 Sep; 32(6):546-52. PubMed ID: 19065332
    [Abstract] [Full Text] [Related]

  • 23. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 24. [Methodological study for detecting gene mutation of family with genotyping of compound heterogenicity of SEA alpha-thalassemia 1 and HbCS].
    Chen J, Luo B, Qi Z, Huo PD, Zhang QS, Wang H.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Jun; 18(3):675-8. PubMed ID: 20561426
    [Abstract] [Full Text] [Related]

  • 25. [Clinical phenotype genotype correlation in children with hemoglobin H disease in Zhuhai area of China].
    Zhou YQ, Xiao QZ, Huang LJ, Xiao GF, Li WD, Zhu LF, Chen ZX, Zhang YM.
    Zhonghua Er Ke Za Zhi; 2004 Sep; 42(9):693-6. PubMed ID: 15482674
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  • 26. Alpha-thalassemia in a selected population of Mexico.
    Casas-Castañeda M, Hernandez-Lugo I, Torres O, Barajas H, Cibrian S, Zamudio G, Villalobos-Arambula AR, Hermosillo-Bañuelos RM, Perea FJ, Ibarra B.
    Rev Invest Clin; 1998 Sep; 50(5):395-8. PubMed ID: 9949669
    [Abstract] [Full Text] [Related]

  • 27. 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 Sep; 22(4):264-8. PubMed ID: 17369692
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  • 32. [Study on genetic diagnosis and prenatal diagnosis of alpha-thalassemia].
    Liu JZ, Wang LR, Huang LJ, Xiao B, Zhou Y.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Feb; 26(2):103-5. PubMed ID: 15921628
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  • 35. A multicenter trial of the effectiveness of zeta-globin enzyme-linked immunosorbent assay and hemoglobin H inclusion body screening for the detection of alpha0-thalassemia trait.
    Lafferty JD, Barth DS, Sheridan BL, McFarlane AG, Halchuk LM, Raby A, Crowther MA.
    Am J Clin Pathol; 2008 Feb; 129(2):309-15. PubMed ID: 18208812
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  • 36. Improvement in the detection of alpha0- and deletional alpha-thalassemia by real-time PCR combined with dissociation curve analysis.
    Liu J, Tang N, Liu Q, Wang L, Han H, Cai R, Wu X, Xiao B.
    Acta Haematol; 2009 Feb; 122(1):17-22. PubMed ID: 19684385
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  • 37. Detection of alpha-thalassemia-1 Southeast Asian type using real-time gap-PCR with SYBR Green1 and high resolution melting analysis.
    Pornprasert S, Phusua A, Suanta S, Saetung R, Sanguansermsri T.
    Eur J Haematol; 2008 Jun; 80(6):510-4. PubMed ID: 18284625
    [Abstract] [Full Text] [Related]

  • 38. Molecular basis of Hb H disease in southwest Iran.
    Yavarian M, Karimi M, Zorai A, Harteveld CL, Giordano PC.
    Hemoglobin; 2005 Jun; 29(1):43-50. PubMed ID: 15768554
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  • 39. A novel fusion gene and a common α(0)-thalassemia deletion cause hemoglobin H disease in a Chinese family.
    Huang JW, Shang X, Zhao Y, Cai R, Zhang XH, Wei XF, Xiong F, Xu XM.
    Blood Cells Mol Dis; 2013 Jun; 51(1):31-4. PubMed ID: 23481460
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  • 40. Molecular basis of alpha-thalassemia in Algeria.
    Mesbah-Amroun H, Rouabhi F, Ducrocq R, Elion J.
    Hemoglobin; 2008 Jun; 32(3):273-8. PubMed ID: 18473243
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