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252 related items for PubMed ID: 12748434

  • 1. The simultaneous presence of alpha- and beta-thalassaemia alleles: a pitfall of thalassaemia screening.
    Law HY, Chee MK, Tan GP, Ng IS.
    Community Genet; 2003; 6(1):14-21. PubMed ID: 12748434
    [Abstract] [Full Text] [Related]

  • 2. Screening of concurrent alpha-thalassaemia 1 in beta-thalassaemia carriers.
    Chong YM, Tan JA, Zubaidah Z, Rahimah A, Kuldip K, George E.
    Med J Malaysia; 2006 Jun; 61(2):217-20. PubMed ID: 16898315
    [Abstract] [Full Text] [Related]

  • 3. The risk of alpha-thalassaemia in offspring of beta-thalassaemia carriers in Hong Kong.
    Lam YH, Ghosh A, Tang MH, Chan V.
    Prenat Diagn; 1997 Aug; 17(8):733-6. PubMed ID: 9267896
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Is routine molecular screening for common alpha-thalassaemia deletions necessary as part of an antenatal screening programme?
    Sorour Y, Heppinstall S, Porter N, Wilson GA, Goodeve AC, Rees D, Wright J.
    J Med Screen; 2007 May; 14(2):60-1. PubMed ID: 17626702
    [Abstract] [Full Text] [Related]

  • 6. [A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].
    Li Q, Li LY, Mo QH.
    Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jan; 28(1):16-9. PubMed ID: 18227017
    [Abstract] [Full Text] [Related]

  • 7. [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; 25(3):256-61. PubMed ID: 18543211
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Alpha-thalassaemia prenatal diagnosis by two PCR-based methods.
    Kleanthous M, Kyriacou K, Kyrri A, Kalogerou E, Vassiliades P, Drousiotou A, Kallikas I, Ioannou P, Angastiniotis M.
    Prenat Diagn; 2001 May; 21(5):413-7. PubMed ID: 11360286
    [Abstract] [Full Text] [Related]

  • 10. A complex haemoglobinopathy diagnosis in a family with both beta zero- and alpha (zero/+)-thalassaemia homozygosity.
    Giordano PC, Harteveld CL, Bok LA, van Delft P, Batelaan D, Beemer FA, Bernini LF.
    Eur J Hum Genet; 1999 May; 7(2):163-8. PubMed ID: 10196699
    [Abstract] [Full Text] [Related]

  • 11. Alpha-thalassaemia in association with beta-thalassaemia patients in Malaysia: a study on the co-inheritance of both disorders.
    Wee YC, Tan KL, Kuldip K, Tai KS, George E, Tan PC, Chia P, Subramaniam R, Yap SF, Tan JA.
    Community Genet; 2008 May; 11(3):129-34. PubMed ID: 18376108
    [Abstract] [Full Text] [Related]

  • 12. Routine screening for α-thalassaemia using an immunochromatographic strip assay for haemoglobin Bart's.
    Prayalaw P, Fucharoen G, Fucharoen S.
    J Med Screen; 2014 Sep; 21(3):120-5. PubMed ID: 24907301
    [Abstract] [Full Text] [Related]

  • 13. Detection and molecular analysis of alpha and beta thalassaemia genes--recent developments in screening protocols.
    Tan J, Tay JS, Wong HB.
    J Singapore Paediatr Soc; 1992 Sep; 34(1-2):53-6. PubMed ID: 1303468
    [Abstract] [Full Text] [Related]

  • 14. Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia.
    Ma ES, Chan AY, Au WY, Yeung YM, Chan LC.
    Haematologica; 2001 Apr; 86(4):432-3. PubMed ID: 11325652
    [Abstract] [Full Text] [Related]

  • 15. Carrier screening for alpha- and beta-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospital.
    Liao C, Mo QH, Li J, Li LY, Huang YN, Hua L, Li QM, Zhang JZ, Feng Q, Zeng R, Zhong HZ, Jia SQ, Cui YY, Xu XM.
    Prenat Diagn; 2005 Feb; 25(2):163-71. PubMed ID: 15712323
    [Abstract] [Full Text] [Related]

  • 16. Cost-effectiveness of prenatal screening for thalassaemia in Hong Kong.
    Leung KY, Lee CP, Tang MH, Lau ET, Ng LK, Lee YP, Chan HY, Ma ES, Chan V.
    Prenat Diagn; 2004 Nov; 24(11):899-907. PubMed ID: 15565640
    [Abstract] [Full Text] [Related]

  • 17. Thalassaemia in pregnancy.
    Leung TY, Lao TT.
    Best Pract Res Clin Obstet Gynaecol; 2012 Feb; 26(1):37-51. PubMed ID: 22079388
    [Abstract] [Full Text] [Related]

  • 18. Premarital screening for beta-thalassaemia in Southern Iran: options for improving the programme.
    Karimi M, Jamalian N, Yarmohammadi H, Askarnejad A, Afrasiabi A, Hashemi A.
    J Med Screen; 2007 Feb; 14(2):62-6. PubMed ID: 17626703
    [Abstract] [Full Text] [Related]

  • 19. 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 Feb; 22(4):264-8. PubMed ID: 17369692
    [Abstract] [Full Text] [Related]

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