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Journal Abstract Search

330 related items for PubMed ID: 15183040

  • 1. Allele frequencies of two polymorphisms associated with the factor IX gene in Iranian population.
    Ghandil P, Ghadiri A, Farhud D, Zeinali S.
    Thromb Res; 2004; 113(5):289-93. PubMed ID: 15183040
    [Abstract] [Full Text] [Related]

  • 2. Factor IX gene haplotypes and its relevance for the indirect genetic analysis of haemophilia B in its Indian perspective.
    Singh M, Singh P.
    Blood Coagul Fibrinolysis; 2008 Jul; 19(5):429-32. PubMed ID: 18600094
    [Abstract] [Full Text] [Related]

  • 3. Carrier detection of haemophilia B by using an intragenic restriction-fragment length polymorphism.
    Bröcker-Vriends AH, Briët E, Quadt R, Bertina RM, van der Linden IK, van de Kamp JJ, Pearson PL, Veltkamp JJ.
    Thromb Haemost; 1985 Aug 30; 54(2):506-9. PubMed ID: 3001965
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  • 4. Carrier detection and prenatal diagnosis in families with haemophilia.
    Shetty S, Ghosh K, Bhide A, Mohanty D.
    Natl Med J India; 2001 Aug 30; 14(2):81-3. PubMed ID: 11396323
    [Abstract] [Full Text] [Related]

  • 5. Molecular analysis of factor IX gene in an Iranian female with severe hemophilia B.
    Karimipoor M, Kokabee L, Kamali E, Karizi SZ, Zeinali S.
    Acta Haematol; 2008 Aug 30; 119(3):151-3. PubMed ID: 18434706
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  • 6. New FACTOR IX linked marker alleles in African Haemophilia B patients.
    Mitchell C, Mitchell CL, Krause A.
    Haemophilia; 2007 Sep 30; 13(5):642-4. PubMed ID: 17880456
    [Abstract] [Full Text] [Related]

  • 7. Detection of carrier status of hemophilia B using DNA markers.
    Ishak R, Zakaria Z.
    Southeast Asian J Trop Med Public Health; 1997 Sep 30; 28(3):629-30. PubMed ID: 9561621
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  • 8. Molecular characterization of hemophilia B in North Indian families: identification of novel and recurrent molecular events in the factor IX gene.
    Mahajan A, Chavali S, Kabra M, Chowdhury MR, Bharadwaj D.
    Haematologica; 2004 Dec 30; 89(12):1498-503. PubMed ID: 15590401
    [Abstract] [Full Text] [Related]

  • 9. DNA polymorphisms for carrier detection of hemophilia in Thailand.
    Chuansumrit A, Goodeve A, Sasanakul W, Peake IR, Pintadit P, Hathirat P, Preston FE, Isarangkul P.
    Southeast Asian J Trop Med Public Health; 1995 Dec 30; 26 Suppl 1():201-6. PubMed ID: 8629107
    [Abstract] [Full Text] [Related]

  • 10. Carrier detection in hemophilia using pedigree analysis coagulation tests and DNA probes.
    de la Salle C, Baas MJ, Grunebaum L, Wiesel ML, Blanco A, Gialeraki R, Mandalaki T, Cazenave JP.
    Nouv Rev Fr Hematol (1978); 1989 Dec 30; 31(3):193-202. PubMed ID: 2575737
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  • 12. Allele frequencies of three factor VIII gene polymorphisms in Iranian populations and their application in hemophilia A carrier detection.
    Azimifar SB, Seyedna SY, Zeinali S.
    Am J Hematol; 2006 May 30; 81(5):335-9. PubMed ID: 16628729
    [Abstract] [Full Text] [Related]

  • 13. Hemophilia B (Christmas disease) variants and carrier detection analyzed by DNA probes.
    Poon MC, Chui DH, Patterson M, Starozik DM, Dimnik LS, Hoar DI.
    J Clin Invest; 1987 Apr 30; 79(4):1204-9. PubMed ID: 2881949
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  • 15. DNA analysis of haemophilia A families from southern France. Experience of a hospital laboratory.
    Aguilar-Martinez P, Fabre N, Navarro R, Schved JF, Gris JC, Romey MC, Demaille J, Claustres M.
    Genet Couns; 1993 Apr 30; 4(4):311-9. PubMed ID: 7906519
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  • 17. Genomic diagnosis of haemophilia A and B in the German Democratic Republic.
    Herrmann FH, Wehnert M, Schröder W.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1990 Apr 30; 117(4):601-7. PubMed ID: 1714866
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  • 19. Diagnosis of hemophilia B carriers using two novel dinucleotide polymorphisms and Hha I RFLP of the factor IX gene in Japanese subjects.
    Toyozumi H, Kojima T, Matsushita T, Hamaguchi M, Tanimoto M, Saito H.
    Thromb Haemost; 1995 Oct 30; 74(4):1009-14. PubMed ID: 8560402
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