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Human Genetics

, Volume 51, Issue 2, pp 231–235 | Cite as

A girl with karyotype 46,XX,del(7)(pter→q32:)

  • Ursula Friedrich
  • Ole Østerballe
  • Stener Stenbjerg
  • Jan Jørgensen
Clinical Case Reports

Keywords

Internal Medicine Metabolic Disease 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. DeGrouchy, J., Turleau, C.: Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band. Humangenetik 24, 197–200 (1974)PubMedGoogle Scholar
  2. Francke, U.: Hageman (Factor XII) locus on 7q? Report of a second case with del(7)q35 and normal factor XII level. Hum. Genet. 45, 363–367 (1978)PubMedGoogle Scholar
  3. 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)PubMedGoogle Scholar
  4. 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)PubMedGoogle Scholar

Copyright information

© Springer-Verlag 1979

Authors and Affiliations

  • Ursula Friedrich
    • 1
  • Ole Østerballe
    • 2
  • Stener Stenbjerg
    • 3
    • 4
  • Jan Jørgensen
    • 3
    • 4
  1. 1.Institute of Human GeneticsUniversity of AarhusÅrhus CDenmark
  2. 2.Department of PediatricsAalborg HospitalAalborgDenmark
  3. 3.The Coagulation LaboratoryUniversity HospitalAarhus CDenmark
  4. 4.Blood Grouping LaboratoryUniversity HospitalAarhus CDenmark

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