96 related articles for article (PubMed ID: 12152672)
1. Is Alu-mediated recombination an important cause of hemophilia?
Sommer SS; Scaringe WA; Hill KA
Thromb Haemost; 2002 Jul; 88(1):3-4. PubMed ID: 12152672
[No Abstract] [Full Text] [Related]
2. First molecular characterization of an unequal homologous alu-mediated recombination event responsible for hemophilia.
Vidal F; Farssac E; Tusell J; Puig L; Gallardo D
Thromb Haemost; 2002 Jul; 88(1):12-6. PubMed ID: 12154809
[TBL] [Abstract][Full Text] [Related]
3. Homeologous recombination between AluSx-sequences as a cause of hemophilia.
Rossetti LC; Goodeve A; Larripa IB; De Brasi CD
Hum Mutat; 2004 Nov; 24(5):440. PubMed ID: 15459970
[TBL] [Abstract][Full Text] [Related]
4. 11 hemophilia A patients without mutations in the factor VIII encoding gene.
Klopp N; Oldenburg J; Uen C; Schneppenheim R; Graw J
Thromb Haemost; 2002 Aug; 88(2):357-60. PubMed ID: 12195713
[No Abstract] [Full Text] [Related]
5. Severe hemophilia A due to a 1.3 kb factor VIII gene deletion including exon 24: homologous recombination between 41 bp within an Alu repeat sequence in introns 23 and 24.
Nakaya SM; Hsu TC; Geraghty SJ; Manco-Johnson MJ; Thompson AR
J Thromb Haemost; 2004 Nov; 2(11):1941-5. PubMed ID: 15550025
[TBL] [Abstract][Full Text] [Related]
6. An Alu insert as the cause of a severe form of hemophilia A.
Sukarova E; Dimovski AJ; Tchacarova P; Petkov GH; Efremov GD
Acta Haematol; 2001; 106(3):126-9. PubMed ID: 11713379
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Analysis of the AluI polymorphism in intron 1 of the human coagulation factor VIII gene: a new marker for the hemophilia A carrier detection].
Surin VL; Luk'ianenko AV; Luchinina IuA
Genetika; 2007 Apr; 43(4):560-6. PubMed ID: 17555134
[TBL] [Abstract][Full Text] [Related]
9. High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype-phenotype correlation.
Citron M; Godmilow L; Ganguly T; Ganguly A
Hum Mutat; 2002 Oct; 20(4):267-74. PubMed ID: 12325022
[TBL] [Abstract][Full Text] [Related]
10. Recurrent inversion with concomitant deletion and insertion events in the coagulation factor VIII gene suggests a new mechanism for X-chromosomal rearrangements causing hemophilia A.
Mühle C; Zenker M; Chuzhanova N; Schneider H
Hum Mutat; 2007 Oct; 28(10):1045. PubMed ID: 17823971
[TBL] [Abstract][Full Text] [Related]
11. Inversion of intron 1 of the factor VIII gene for direct molecular diagnosis of hemophilia A.
Tizzano EF; Cornet M; Baiget M
Haematologica; 2003 Jan; 88(1):118-20. PubMed ID: 12551839
[No Abstract] [Full Text] [Related]
12. Inhibitors of factor VIII in hemophilia.
Yang G; Yao L; Lu Z
N Engl J Med; 2009 Jul; 361(3):309; author reply 310. PubMed ID: 19610161
[No Abstract] [Full Text] [Related]
13. Reduced clinical severity in a mutationally well-characterized cohort of severe hemophilia with associated thrombophilia.
Shetty S; Ghosh K
Am J Clin Pathol; 2008 Jul; 130(1):84-7; quiz 146. PubMed ID: 18550475
[TBL] [Abstract][Full Text] [Related]
14. Major disorganization of factor VIII gene as a cause of severe hemophilia A in Indian patients.
Shetty S; Ghosh K; Mohanty D
Am J Hematol; 2004 May; 76(1):96. PubMed ID: 15114612
[No Abstract] [Full Text] [Related]
15. The Malmö International Brother Study (MIBS). Genetic defects and inhibitor development in siblings with severe hemophilia A.
Mannhalter C
Haematologica; 2005 Jul; 90(7):869A. PubMed ID: 15996920
[No Abstract] [Full Text] [Related]
16. Characterization of a causative mutation of hemophilia A identified in the promoter region of the factor VIII gene (F8).
Dai L; Cutler JA; Savidge GF; Mitchell MJ
J Thromb Haemost; 2008 Jan; 6(1):193-5. PubMed ID: 17944985
[No Abstract] [Full Text] [Related]
17. Inhibitors of factor VIII in hemophilia.
Eckhardt CL; Kamphuisen PW; Fijnvandraat K
N Engl J Med; 2009 Jul; 361(3):309; author reply 310. PubMed ID: 19610163
[No Abstract] [Full Text] [Related]
18. [Molecular analysis of hemophilia A].
Shima M
Rinsho Ketsueki; 1998 Feb; 39(2):137-8. PubMed ID: 9545826
[No Abstract] [Full Text] [Related]
19. Exon skipping partially restores factor VIII coagulant activity in patients with mild hemophilia A with exon 13 duplication.
Acquila M; Pasino M; Lanza T; Molinari AC; Rosano C; Bicocchi MP
Haematologica; 2005 Jul; 90(7):997-9. PubMed ID: 15996947
[TBL] [Abstract][Full Text] [Related]
20. Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N.
Berber E; Fidanci ID; Un C; El-Maarri O; Aktuglu G; Gurgey A; Celkan T; Meral A; Oldenburg J; Graw J; Akar N; Caglayan H
Haemophilia; 2006 Jul; 12(4):398-400. PubMed ID: 16834740
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
