Skip to main content
SpringerLink
Log in

Hageman (factor XII) locus on 7q?

Report of a second case with del(7)q35 and normal factor XII level

  • Letter to the Editors
  • Published:
Human Genetics Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

References

  • Bennett, B., Ratnoff, O. D., Holt, J. B., Roberts, H. R.: Hageman trait (factor XII deficiency): a probable second genotype inherited as an autosomal dominant characteristic. Blood 40, 412–415 (1972)

    PubMed  Google Scholar 

  • Biederman, B., Bowen, P.: Balanced t(8;9)(q12;q33)pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long arm of chromosome 7. Hum. Genet. 41, 101–107 (1978)

    Article  PubMed  Google Scholar 

  • Biggs, R. (ed.): Human blood coagulation, hemostasis and thrombosis, 2nd ed., Appendices, K. W. E. Denson (ed.). Blackwell Scientific Corp. 1976

  • DeGrouchy, J., Turleau, C.: Tentative localization of a Hageman (factor XII) locus on 7q, probably the 7q35 band. Humangenetik 24, 197–200 (1974)

    PubMed  Google Scholar 

  • Harris, E. L., Wappner, R. S., Palmer, C. G., Hall, B., Dinno, N., Seashore, M. R., Breg, W. R.: 7q deletion syndrome (7q32→7qter). Clin. Genet. 12, 233–238 (1977)

    PubMed  Google Scholar 

  • Hougie, C.: Von Willebrand disease San Diego. Lancet 1977 I, 93–94

  • Kasper, C. K., Whissell Buenchy, D. Y. E., Aggeler, P. M.: Hageman factor (factor XII) in an affected kindred and in normal adults. Br. J. Haematol. 14, 543–555 (1968)

    PubMed  Google Scholar 

  • Kousseff, B., Hsu, L. Y. F., Paciuc, S., Hirschhorn, K.: A partial long arm deletion of chromosome 7: 46,XY,del(7)(q32). J. Med. Genet. 14, 144–147 (1977)

    PubMed  Google Scholar 

  • Veltkamp, J. J., Drion, E. F., Loeliger, E. A.: Detection of the carrier state in hereditary coagulation disorders. Thromb. Diath. Haemorrh. 19, 403–422 (1968)

    PubMed  Google Scholar 

  • Veltkamp, J. J., van Tilburg, N. H., Muller, H. P.: Von Willebrand disease San Diego. Lancet 1976 II, 909

  • Yunis, J. J.: High resolution of human chromosomes. Science 191, 1268–1270 (1976)

    PubMed  Google Scholar 

Download references

Author information

Author notes

  1. Uta Francke

    Present address: Department of Human Genetics, Yale University, 333 Cedar Street, 06510, New Haven, Connecticut, USA

Authors and Affiliations

  1. Department of Pediatrics, University of California San Diego School of Medicine, USA

    Uta Francke

  2. San Diego Children's Hospital and Health Center, USA

    Uta Francke

Authors
  1. Uta Francke
    View author publications

    You can also search for this author in PubMed Google Scholar

Rights and permissions

Reprints and permissions

About this article

Cite this article

Francke, U. Hageman (factor XII) locus on 7q?. Hum Genet 45, 363–367 (1978). https://doi.org/10.1007/BF00278736

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00278736

Keywords

Search

Navigation