메뉴 건너뛰기




Volumn 10, Issue 6, 2004, Pages 751-755

Mutation analysis in F9 gene of 17 families with haemophilia B from Iran [4]

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; BLOOD CLOTTING FACTOR 9; CYTOSINE; GUANINE; THYMINE;

EID: 11144339953     PISSN: 13518216     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2004.01041.x     Document Type: Letter
Times cited : (4)

References (13)
  • 1
    • 0027244515 scopus 로고
    • Molecular biology of haemophilia B
    • Roberts HR. Molecular biology of haemophilia B. Thromb Haemost 1993; 70: 1-9.
    • (1993) Thromb. Haemost. , vol.70 , pp. 1-9
    • Roberts, H.R.1
  • 2
    • 0036218048 scopus 로고    scopus 로고
    • Haemophilia A and haemophilia B: Molecular insights
    • Bowen DJ. Haemophilia A and haemophilia B: molecular insights. J Clin Pathol Mol Pathol 2002; 55: 1-18.
    • (2002) J. Clin. Pathol. Mol. Pathol. , vol.55 , pp. 1-18
    • Bowen, D.J.1
  • 3
    • 0031915612 scopus 로고    scopus 로고
    • Laboratory methods for the genetic diagnosis of bleeding disorders
    • Goodeve AC. Laboratory methods for the genetic diagnosis of bleeding disorders. Clin Lab Haem 1998; 20: 3-19.
    • (1998) Clin. Lab. Haem. , vol.20 , pp. 3-19
    • Goodeve, A.C.1
  • 4
    • 0032997912 scopus 로고    scopus 로고
    • Start of UK confidential haemophilia database: Analysis of 142 patients by solid phase fluorescent chemical cleavage of mismatch
    • and the Haemophilia Centres
    • Waseem NH, Bagnll R, Green PM, Giannelli F and the Haemophilia Centres. Start of UK confidential haemophilia database: analysis of 142 patients by solid phase fluorescent chemical cleavage of mismatch. Thromb Haemost 1999; 81: 900-5.
    • (1999) Thromb. Haemost. , vol.81 , pp. 900-905
    • Waseem, N.H.1    Bagnll, R.2    Green, P.M.3    Giannelli, F.4
  • 5
    • 0024756969 scopus 로고
    • Rapid and sensitive detection point mutations and DNA polymorphisms using the polymerase chain reaction
    • Orita M, Susuki Y, Sekiya T, Hayashi K. Rapid and sensitive detection point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics 1989; 5: 874-9.
    • (1989) Genomics , vol.5 , pp. 874-879
    • Orita, M.1    Susuki, Y.2    Sekiya, T.3    Hayashi, K.4
  • 6
    • 0023476285 scopus 로고
    • Detection and localization of single base changes by denaturing gel electrophoresis
    • Myers RM, Manitas T, Lerman LS. Detection and localization of single base changes by denaturing gel electrophoresis. Meth Enzymol 1987; 155: 501-27.
    • (1987) Meth. Enzymol. , vol.155 , pp. 501-527
    • Myers, R.M.1    Manitas, T.2    Lerman, L.S.3
  • 7
    • 0033057879 scopus 로고    scopus 로고
    • A rapid method for haemophilia B mutation detection using confirmation sensitive gel electrophoresis
    • Hinks JL, Winship MJ, Makris M, Preston FE, Peak IR, Goodeve AC. A rapid method for haemophilia B mutation detection using confirmation sensitive gel electrophoresis. Br J Haematol 1998; 104: 915-8.
    • (1998) Br. J. Haematol. , vol.104 , pp. 915-918
    • Hinks, J.L.1    Winship, M.J.2    Makris, M.3    Preston, F.E.4    Peak, I.R.5    Goodeve, A.C.6
  • 8
    • 0035073619 scopus 로고    scopus 로고
    • Mutation profiling in haemophilia A
    • Oldenburg J. Mutation profiling in haemophilia A. Thromb Haemost 2001; 85: 577-9.
    • (2001) Thromb. Haemost. , vol.85 , pp. 577-579
    • Oldenburg, J.1
  • 9
    • 0036210959 scopus 로고    scopus 로고
    • Carrier detection and prenatal diagnosis in haemophilia in India: Realities and challenges
    • Ghosh K, Shetty S, Pawar A, Mohanty D. Carrier detection and prenatal diagnosis in haemophilia in India: realities and challenges. Haemophilia 2002; 8: 51-5.
    • (2002) Haemophilia , vol.8 , pp. 51-55
    • Ghosh, K.1    Shetty, S.2    Pawar, A.3    Mohanty, D.4
  • 11
    • 0037277123 scopus 로고    scopus 로고
    • Carrier testing and prenatal diagnosis of haemophilia B by SSCP in an Iranian family
    • Karimipoor M, Zeinali S, Lak M, Safaee R. Carrier testing and prenatal diagnosis of haemophilia B by SSCP in an Iranian family. Haemophilia 2003; 9: 116-8.
    • (2003) Haemophilia , vol.9 , pp. 116-118
    • Karimipoor, M.1    Zeinali, S.2    Lak, M.3    Safaee, R.4
  • 12
    • 0035022048 scopus 로고    scopus 로고
    • Haemophilia B mutations in Sweden: A population-based study of mutational heterogeneity
    • Lung R, Pretini P, Tengborn L, Sjörin E. Haemophilia B mutations in Sweden: a population-based study of mutational heterogeneity. Br J Haematol 2001; 113: 81-6.
    • (2001) Br. J. Haematol. , vol.113 , pp. 81-86
    • Lung, R.1    Pretini, P.2    Tengborn, L.3    Sjörin, E.4
  • 13
    • 0345701968 scopus 로고    scopus 로고
    • Molecular pathology of haemophilia B in Turkish patients: Identification of a large deletion and 33 independent point mutations
    • Onay UV, Kavakli K, Kiliç Y et al. Molecular pathology of haemophilia B in Turkish patients: identification of a large deletion and 33 independent point mutations. Br J Haematol 2003; 120: 656-59.
    • (2003) Br. J. Haematol. , vol.120 , pp. 656-659
    • Onay, U.V.1    Kavakli, K.2    Kiliç, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.