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Journal Abstract Search

115 related items for PubMed ID: 21649803

  • 1. Analysis of five polymorphic DNA markers for indirect genetic diagnosis of haemophilia A in the Brazilian population.
    Massaro JD, Wiezel CE, Muniz YC, Rego EM, de Oliveira LC, Mendes-Junior CT, Simões AL.
    Haemophilia; 2011 Sep; 17(5):e936-43. PubMed ID: 21649803
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  • 7. Carrier analysis and prenatal diagnosis of haemophilia A in North India.
    Pandey GS, Phadke SR, Mittal B.
    Int J Mol Med; 2002 Nov; 10(5):661-4. PubMed ID: 12373312
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  • 8. Identification of new dinucleotide-repeat polymorphisms in factor VIII gene using fluorescent PCR.
    Kim JW, Park SY, Kim YM, Kim JM, Kim DJ, Ryu HM.
    Haemophilia; 2005 Jan; 11(1):38-42. PubMed ID: 15660987
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  • 10. Carrier detection and prenatal diagnosis in families with haemophilia.
    Shetty S, Ghosh K, Bhide A, Mohanty D.
    Natl Med J India; 2001 Jan; 14(2):81-3. PubMed ID: 11396323
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  • 13. High-resolution combined linkage physical map of short tandem repeat loci on human chromosome band Xq28 for indirect haemophilia A carrier detection.
    Machado FB, Medina-Acosta E.
    Haemophilia; 2009 Jan; 15(1):297-308. PubMed ID: 18752533
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  • 14. Molecular diagnosis in haemophilia A.
    Pandey GS, Mittal B.
    J Postgrad Med; 2001 Jan; 47(4):274-80. PubMed ID: 11832649
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  • 18. Carrier detection and prenatal diagnosis of hemophilia in developing countries.
    Peyvandi F.
    Semin Thromb Hemost; 2005 Nov; 31(5):544-54. PubMed ID: 16276463
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  • 19. Recombinant DNA methods in hemophilia A: carrier detection and prenatal diagnosis.
    Sadler JE.
    Semin Thromb Hemost; 1990 Oct; 16(4):341-7. PubMed ID: 2126393
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  • 20. Application of intron 9 and intron 25 dinucleotide repeats of the factor VIII gene for carrier diagnosis in haemophilia A.
    Venceslá A, Baena M, Fares Taie L, Cornet M, Baiget M, Tizzano EF.
    Haemophilia; 2008 May; 14(3):489-93. PubMed ID: 18384354
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