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Volumn 54, Issue 4, 1997, Pages 271-275

Factor VIII and IX gene polymorphisms and carrier analysis in Indian population

Author keywords

Carrier detection; Hemophilia; Polymorphism

Indexed keywords

BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9;

EID: 0030934641     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8652(199704)54:4<271::AID-AJH2>3.0.CO;2-S     Document Type: Article
Times cited : (40)

References (12)
  • 3
    • 0023242425 scopus 로고
    • An improved method of prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A
    • Kogan SC, Doherty M, Gitschier J: An improved method of prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A. N Engl J Med 317:985, 1987.
    • (1987) N Engl J Med , vol.317 , pp. 985
    • Kogan, S.C.1    Doherty, M.2    Gitschier, J.3
  • 4
    • 0024500697 scopus 로고
    • Detection of polymorphisms at cytosine phosphoguanidine dinuclcotides and diagnosis of haemophilia B carriers
    • Winship PR, Rees DJG, Alkan M: Detection of polymorphisms at cytosine phosphoguanidine dinuclcotides and diagnosis of haemophilia B carriers. Lancet 1:631, 1989.
    • (1989) Lancet , vol.1 , pp. 631
    • Winship, P.R.1    Rees, D.J.G.2    Alkan, M.3
  • 5
    • 0025763422 scopus 로고
    • Facile and rapid analysis of three DNA polymorphisms within the human factor IX gene using the polymerase chain reaction
    • Bowen DJ, Thomas P, Webb CE, Bignell P, Peake IR, Bloom AL: Facile and rapid analysis of three DNA polymorphisms within the human factor IX gene using the polymerase chain reaction. Br J Haematol 77:559, 1991.
    • (1991) Br J Haematol , vol.77 , pp. 559
    • Bowen, D.J.1    Thomas, P.2    Webb, C.E.3    Bignell, P.4    Peake, I.R.5    Bloom, A.L.6
  • 6
    • 0021760755 scopus 로고
    • Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms
    • Winship PR, Anson DS, Rizza CR, Brownlee GG: Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms. Nucleic Acids Res 12:8861, 1984.
    • (1984) Nucleic Acids Res , vol.12 , pp. 8861
    • Winship, P.R.1    Anson, D.S.2    Rizza, C.R.3    Brownlee, G.G.4
  • 9
    • 0025950099 scopus 로고
    • The varying frequencies of five DNA polymorphisms of X-linked coagulant factor IX in eight ethnic groups
    • Graham JB, Kunkel GR, Egilmez NK, Wallmark A, Fowlkrs DM, Lord ST: The varying frequencies of five DNA polymorphisms of X-linked coagulant factor IX in eight ethnic groups. Am J Hum Genet 49:537, 1991.
    • (1991) Am J Hum Genet , vol.49 , pp. 537
    • Graham, J.B.1    Kunkel, G.R.2    Egilmez, N.K.3    Wallmark, A.4    Fowlkrs, D.M.5    Lord, S.T.6
  • 10
    • 0027520025 scopus 로고
    • Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A
    • Lakich D, Kazazian HH, Antonarakis SE, Gitschier J: Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A. Nat Genet 5:236, 1993.
    • (1993) Nat Genet , vol.5 , pp. 236
    • Lakich, D.1    Kazazian, H.H.2    Antonarakis, S.E.3    Gitschier, J.4
  • 11
    • 0027376685 scopus 로고
    • Characteristic mRNa abnormality found in half the patients with severe haemophilia a is due to large DNa inversions
    • Naylor J, Brinke A, Hassock S, Green P, Gianelli F: Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions. Hum Mol Genet 2:1773, 1993.
    • (1993) Hum Mol Genet , vol.2 , pp. 1773
    • Naylor, J.1    Brinke, A.2    Hassock, S.3    Green, P.4    Gianelli, F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.