These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 9569180)

  • 41. [Analysis of X ba I polymorphism of FVIII gene and its application on prenatal diagnosis for hemophilia A].
    Wang ZY; Liang Y; Zhou Y; Xiao B; Liu JZ
    Zhonghua Xue Ye Xue Za Zhi; 2006 Mar; 27(3):170-2. PubMed ID: 16792918
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Detection of 95 novel mutations in coagulation factor VIII gene F8 responsible for hemophilia A: results from a single institution.
    Guillet B; Lambert T; d'Oiron R; Proulle V; Plantier JL; Rafowicz A; Peynet J; Costa JM; Bendelac L; Laurian Y; Lavergne JM
    Hum Mutat; 2006 Jul; 27(7):676-85. PubMed ID: 16786531
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Haemophilia A, factor VIII intron 22 inversion screening using subcycling-PCR.
    Kilian NL; Pospisil V; Hanrahan V
    Thromb Haemost; 2006 Apr; 95(4):746-7. PubMed ID: 16601851
    [No Abstract]   [Full Text] [Related]  

  • 44. 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; 89(12):1498-503. PubMed ID: 15590401
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Inversion of intron 22 in isolated cases of severe hemophilia A.
    Tizzano EF; Domènech M; Baiget M
    Thromb Haemost; 1995 Jan; 73(1):6-9. PubMed ID: 7740498
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Mutational spectrum of F8 gene and prothrombotic gene variants in haemophilia A patients from Southern Italy.
    Sanna V; Zarrilli F; Nardiello P; D'Argenio V; Rocino A; Coppola A; DI Minno G; Castaldo G
    Haemophilia; 2008 Jul; 14(4):796-803. PubMed ID: 18459951
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Mutational-screening in the factor VIII gene resulting in the identification of three novel mutations, one of which is a donor splice mutation. Mutations in brief no. 245. Online.
    Möller-Morlang K; Tavassoli K; Eigel A; Pollmann H; Horst J
    Hum Mutat; 1999; 13(6):504. PubMed ID: 10408784
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Use of Intron 1 and 22 inversions and linkage analysis in carrier detection of hemophilia A in Indians.
    Ahmed R; Kannan M; Biswas A; Ranjan R; Choudhry VP; Saxena R
    Clin Chim Acta; 2006 Mar; 365(1-2):109-12. PubMed ID: 16129422
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A.
    Lakich D; Kazazian HH; Antonarakis SE; Gitschier J
    Nat Genet; 1993 Nov; 5(3):236-41. PubMed ID: 8275087
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A.
    Bogdanova N; Markoff A; Pollmann H; Nowak-Göttl U; Eisert R; Wermes C; Todorova A; Eigel A; Dworniczak B; Horst J
    Hum Mutat; 2005 Sep; 26(3):249-54. PubMed ID: 16086318
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Analysis of large structural changes of the factor VIII gene, involving intron 1 and 22, in severe hemophilia A.
    Andrikovics H; Klein I; Bors A; Nemes L; Marosi A; Váradi A; Tordai A
    Haematologica; 2003 Jul; 88(7):778-84. PubMed ID: 12857556
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Carrier testing strategy in haemophilia A using two polymorphic DNA probes of the factor VIII gene.
    Intrator S; Noel B; Lucotte G
    Exp Hematol; 1987 Mar; 15(3):304-5. PubMed ID: 3102274
    [No Abstract]   [Full Text] [Related]  

  • 53. The spectrum of mutations in Southern Spanish patients with hemophilia A and identification of 28 novel mutations.
    Fernández-López O; García-Lozano JR; Núñez-Vázquez R; Pérez-Garrido R; Núñez-Roldán A
    Haematologica; 2005 May; 90(5):707-10. PubMed ID: 15921397
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A rapid multifluorescent polymerase chain reaction for genetic counselling in Chinese haemophilia A families.
    Fang Y; Wang XF; Dai J; Wang HL
    Haemophilia; 2006 Jan; 12(1):62-7. PubMed ID: 16409177
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Factor VIII gene inversions and polymorphisms in Brazilian patients with haemophilia A: carrier detection and prenatal diagnosis.
    Soares RP; Chamone DA; Bydlowski SP
    Haemophilia; 2001 May; 7(3):299-305. PubMed ID: 11380635
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Protein truncation test: detection of severe haemophilia a mutation and analysis of factor VIII transcripts.
    Maugard C; Tuffery S; Aguilar-Martinez P; Schved JF; Gris JC; Demaille J; Claustres M
    Hum Mutat; 1998; 11(1):18-22. PubMed ID: 9450898
    [No Abstract]   [Full Text] [Related]  

  • 57. Genetic counseling of hemophilia carriers.
    Ljung R; Tedgård U
    Semin Thromb Hemost; 2003 Feb; 29(1):31-6. PubMed ID: 12640562
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype.
    Margaglione M; Castaman G; Morfini M; Rocino A; Santagostino E; Tagariello G; Tagliaferri AR; Zanon E; Bicocchi MP; Castaldo G; Peyvandi F; Santacroce R; Torricelli F; Grandone E; Mannucci PM;
    Haematologica; 2008 May; 93(5):722-8. PubMed ID: 18387975
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocols.
    Markoff A; Sormbroen H; Bogdanova N; Preisler-Adams S; Ganev V; Dworniczak B; Horst J
    Eur J Hum Genet; 1998; 6(2):145-50. PubMed ID: 9781059
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Spectrum of causative mutations in patients with haemophilia A in Austria.
    Reitter S; Sturn R; Horvath B; Freitag R; Male C; Muntean W; Streif W; Pabinger I; Mannhalter C;
    Thromb Haemost; 2010 Jul; 104(1):78-85. PubMed ID: 20431853
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.