Thromb Haemost 1985; 54(03): 728
DOI: 10.1055/s-0038-1660111
Letter to the Editor
Schattauer GmbH Stuttgart

Homozygous Hemophilia A in a Female

P Sié
*   The Laboratoire d’Hémostase, Centre de Transfusion Sanguine, 31052 Toulouse Cedex, France
,
C Caranobe
*   The Laboratoire d’Hémostase, Centre de Transfusion Sanguine, 31052 Toulouse Cedex, France
,
M Benalioua
**   The Centre Emir Abdel Kader, Oran, Algérie
,
B Boneu
*   The Laboratoire d’Hémostase, Centre de Transfusion Sanguine, 31052 Toulouse Cedex, France
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Received 28. Mai 1985

Accepted 03. Juli 1985

Publikationsdatum:
19. Juli 2018 (online)

 
  • References

  • 1 Graham JB. Mode of inheritance and current research. Handbook of hemophilia Excerpta Medica; Amsterdam: 1975. p 175-85
  • 2 Morita H, Kagami M, Ebata Y, Yoshimura H. The occurrence of homozygous hemophilia in the female. Acta Haematol 1971; 45: 112-9
  • 3 Joist JH, Bouhasin JD, Roodman S. Classical hemophilia A in a female. Acta Haematol 1977; 58: 94-102
  • 4 Peake IR, Bloom AL, Giddings JC, Ludlam CA. An immunoradiometric assay for procoagulant factor VIII antigen. Results in haemophilia von Willebran’s disease and fetal plasma and serum. Br J Haematol 1979; 42: 269-81
  • 5 Seabright M. A rapid banding technique for human chromosome. Lancet 1971; 2: 971-2
  • 6 Graham JB, Barrow ES, Flyer P, Dawson DV, Elston RC. Identifying carriers of mild hemophilia. Br J Haematol 1980; 44: 671-8
  • 7 Graham JB, Barrow ES, Elston RC. Lyonisation in hemophilia: a case of error in direct detection of heterozygous carriers. Ann NY Acad Sci 1975; 240: 141-6