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 *

150 related articles for article (PubMed ID: 7669670)

  • 1. Severe haemophilia A in a female resulting from two de novo factor VIII mutations.
    Windsor S; Lyng A; Taylor SA; Ewenstein BM; Neufeld EJ; Lillicrap D
    Br J Haematol; 1995 Aug; 90(4):906-9. PubMed ID: 7669670
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Female haemophiliac homozygous for the factor VIII intron 22 inversion mutation, with transcriptional inactivation of one of the factor VIII alleles.
    David D; Morais S; Ventura C; Campos M
    Haemophilia; 2003 Jan; 9(1):125-30. PubMed ID: 12558791
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.
    Seeler RA; Vnencak-Jones CL; Bassett LM; Gilbert JB; Michaelis RC
    Haemophilia; 1999 Nov; 5(6):445-9. PubMed ID: 10583534
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Severe haemophilia A in a female resulting from an inherited gross deletion and a de novo codon deletion in the F8 gene.
    Venceslá A; Fuentes-Prior P; Baena M; Quintana M; Baiget M; Tizzano EF
    Haemophilia; 2008 Sep; 14(5):1094-8. PubMed ID: 18665854
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inversions in the factor VIII gene: improvement of carrier detection and prenatal diagnosis in Dutch haemophilia A families.
    Deutz-Terlouw PP; Losekoot M; Olmer R; Pieneman WC; de Vries-v d Weerd S; Briët E; Bakker E
    J Med Genet; 1995 Apr; 32(4):296-300. PubMed ID: 7643361
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Factor VIII gene inversions in severe hemophilia A: results of an international consortium study.
    Antonarakis SE; Rossiter JP; Young M; Horst J; de Moerloose P; Sommer SS; Ketterling RP; Kazazian HH; Négrier C; Vinciguerra C; Gitschier J; Goossens M; Girodon E; Ghanem N; Plassa F; Lavergne JM; Vidaud M; Costa JM; Laurian Y; Lin SW; Lin SR; Shen MC; Lillicrap D; Taylor SA; Windsor S; Valleix SV; Nafa K; Sultan Y; Delpech M; Vnencak-Jones CL; Phillips JA; Ljung RC; Koumbarelis E; Gialeraki A; Mandalaki T; Jenkins PV; Collins PW; Pasi KJ; Goodeve A; Peake I; Preston FE; Schwartz M; Scheibel E; Ingerslev J; Cooper DN; Millar DS; Kakkar VV; Giannelli F; Naylor JA; Tizzano EF; Baiget M; Domenech M; Altisent C; Tusell J; Beneyto M; Lorenzo JI; Gaucher C; Mazurier C; Peerlinck K; Matthijs G; Cassiman JJ; Vermylen J; Mori PG; Acquila M; Caprino D; Inaba H
    Blood; 1995 Sep; 86(6):2206-12. PubMed ID: 7662970
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Origin of mutation in sporadic cases of haemophilia A.
    Ljung RC; Sjörin E
    Br J Haematol; 1999 Sep; 106(4):870-4. PubMed ID: 10519986
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inversions of the factor VIII gene in Swedish patients with severe haemophilia A.
    Ljung R; Sjörin E
    Eur J Haematol; 1995 May; 54(5):310-3. PubMed ID: 7781755
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two de novo factor VIII gene mutations in the family of an isolated severe haemophilia A patient.
    Kapsimali Z; Pavlova A; Pergantou H; Adamtziki E; Oldenburg J; Platokouki H
    Haemophilia; 2012 Jan; 18(1):e3-4. PubMed ID: 21740484
    [No Abstract]   [Full Text] [Related]  

  • 10. De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism.
    Oldenburg J; Rost S; El-Maarri O; Leuer M; Olek K; Müller CR; Schwaab R
    Blood; 2000 Oct; 96(8):2905-6. PubMed ID: 11023529
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots.
    Youssoufian H; Kazazian HH; Phillips DG; Aronis S; Tsiftis G; Brown VA; Antonarakis SE
    Nature; 1986 Nov 27-Dec 3; 324(6095):380-2. PubMed ID: 3097553
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A pericentric inversion of chromosome X disrupting
    Xin Y; Zhou J; Ding Q; Chen C; Wu X; Wang X; Wang H; Jiang X
    J Clin Pathol; 2017 Aug; 70(8):656-661. PubMed ID: 28073995
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical correlates among 49 families with hemophilia A and factor VIII gene inversions.
    Weinmann AF; Schoof JM; Thompson AR
    Am J Hematol; 1996 Mar; 51(3):192-9. PubMed ID: 8619399
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Female hemophilia A heterozygous for a de novo frameshift and a novel missense mutation of factor VIII.
    Cai XH; Wang XF; Dai J; Fang Y; Ding QL; Xie F; Wang HL
    J Thromb Haemost; 2006 Sep; 4(9):1969-74. PubMed ID: 16805874
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening for inversions in the factor VIII (F8) gene causing severe haemophilia A.
    Millar DS; Kakkar VV; Cooper DN
    Blood Coagul Fibrinolysis; 1994 Apr; 5(2):239-42. PubMed ID: 8054456
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Factor VIII gene inversions and an XbaI polymorphism: nonradioactive detection and clinical usage.
    Liu ML; Thompson AR
    Haemophilia; 1999 Jan; 5(1):26-31. PubMed ID: 10215944
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female.
    Favier R; Lavergne JM; Costa JM; Caron C; Mazurier C; Viémont M; Delpech M; Valleix S
    Blood; 2000 Dec; 96(13):4373-5. PubMed ID: 11110718
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Large DNA inversions, deletions, and TaqI site mutations in severe haemophilia A.
    Figueiredo MS; Tavella MH; Simões BP
    Hum Genet; 1994 Nov; 94(5):473-8. PubMed ID: 7959679
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of intron 1 and 22 inversion mutations in the factor VIII gene of 124 Iranian families with severe haemophilia A.
    Rastegar Lari G; Enayat MS; Arjang Z; Lavergne JM; Ala F
    Haemophilia; 2004 Jul; 10(4):410-1. PubMed ID: 15230960
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.