Advertisement

Human Genetics

, Volume 32, Issue 1, pp 105–107 | Cite as

Does full monosomy 21 exist?

A comment to the paper: A male infant with monosomy 21 by Y. Kaneko, T. Ikeuchi, M. Sasaki, Y. Satake and S. Kuwajima Humangenetik 29, 1–7 (1975)
  • A. Schinzel
Letters to the Editors

Keywords

Internal Medicine Metabolic Disease Full Monosomy 
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.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Bauld, R., Sutherland, G. R., Bain, A. D.: Chromosome studies in investigation of stillbirths and neonatal deaths. Arch. Dis. Childh.49, 782–788 (1974)Google Scholar
  2. Cooksley, W. G. E., Firouz-Abadi, A., Wallace, D. C.: Monosomy of a “G” autosome in a 22-year-old female. Med. J. Aust.2, 178–180 (1973)Google Scholar
  3. Gripenberg, U., Elfving, J., Gripenberg, L.: A 45,XX,21-child: attempt at a cytological and clinical interpretation of the karyotype. J. med. Genet.9, 110–115 (1972)Google Scholar
  4. Halloran, K. H., Breg, W. R., Mahoney, M. J.: 21 monosomy in a retarded female infant. J. med. Genet.11, 386–389 (1974)Google Scholar
  5. Kaneko, Y., Ikeuchi, T., Sasaki, M., Kuwajima, S.: A male infant with monosomy 21. Humangenetik29, 1–7 (1975)Google Scholar
  6. Niebuhr, E., Ottosen, J.: Ring chromosome D(13) associated with multiple congenital malformations. Ann. Génét.16, 157–166 (1973)Google Scholar

Copyright information

© Springer-Verlag 1976

Authors and Affiliations

  • A. Schinzel
    • 1
  1. 1.Division of Medical Genetics, Department of PediatricsUniversity of ZurichSwitzerland

Personalised recommendations