This is a preview of subscription content, log in to check access.
Buy single article
Instant access to the full article PDF.
Price includes VAT for USA
Subscribe to journal
Immediate online access to all issues from 2019. Subscription will auto renew annually.
This is the net price. Taxes to be calculated in checkout.
Bauld, R., Sutherland, G. R., Bain, A. D.: Chromosome studies in investigation of stillbirths and neonatal deaths. Arch. Dis. Childh.49, 782–788 (1974)
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)
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)
Halloran, K. H., Breg, W. R., Mahoney, M. J.: 21 monosomy in a retarded female infant. J. med. Genet.11, 386–389 (1974)
Kaneko, Y., Ikeuchi, T., Sasaki, M., Kuwajima, S.: A male infant with monosomy 21. Humangenetik29, 1–7 (1975)
Niebuhr, E., Ottosen, J.: Ring chromosome D(13) associated with multiple congenital malformations. Ann. Génét.16, 157–166 (1973)
About this article
Cite this article
Schinzel, A. Does full monosomy 21 exist?. Hum Genet 32, 105–107 (1976). https://doi.org/10.1007/BF00569984
- Internal Medicine
- Metabolic Disease
- Full Monosomy