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PUBMED FOR HANDHELDS

Journal Abstract Search

468 related items for PubMed ID: 1982946

  • 1. Carrier detection and prenatal diagnosis in haemophilia A and B.
    Chistolini A, Papacchini M, Mazzucconi MG, La Verde G, Arcieri R, Ferrari A, Paesano R, Pachi A, Mariani G.
    Haematologica; 1990; 75(5):424-8. PubMed ID: 1982946
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  • 4. Molecular genetics and counselling in haemophilia.
    Peake I.
    Thromb Haemost; 1995 Jul; 74(1):40-4. PubMed ID: 8578494
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  • 13. Haemophilia: strategies for carrier detection and prenatal diagnosis.
    Peake IR, Lillicrap DP, Boulyjenkov V, Briet E, Chan V, Ginter EK, Kraus EM, Ljung R, Mannucci PM, Nicolaides K.
    Bull World Health Organ; 1993 Jul; 71(3-4):429-58. PubMed ID: 8324863
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  • 14. Carrier detection for prenatal diagnosis of hemophilia A in Italian families.
    Cappello N, Restagno G, Garnerone S, Gennaro C, Perugini L, Rendine S, Piazza A, Carbonara A.
    Haematologica; 1992 Jul; 77(4):302-6. PubMed ID: 1358771
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  • 20. Hemophilia A carrier detection by restriction fragment length polymorphism analysis and discriminant analysis based on ELISA of factor VIII and vWf.
    Poon MC, Hoar DI, Low S, Pon JK, Anand S, Sinclair GD.
    J Lab Clin Med; 1992 Jun; 119(6):751-62. PubMed ID: 1350611
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