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Particular Aberration of G-Group Chromosomes

Published online by Cambridge University Press:  01 August 2014

P. Grünwald  and
F. Schweikhardt
P. Grünwald*
Affiliation:
Institut für Humangenetik derUniversität Düsseldorf
F. Schweikhardt*
Affiliation:
Institut für Humangenetik derUniversität Düsseldorf
*
Pfeifferstrasse 20, 4 Düsseldorf, Deutschland
Höpker-Aschoff-Weg 26, 49 Herford, Westf., Deutschland

Summary

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Three clinically atypical cases of Down S. and cerebral idiocy are described, showing peculiar chromosomal deviations and of difficult diagnosis. One more case is described, partly showing Marfan S. symptomatology with a duplication of the satellite-region of a G-Chromosome. This chromosomal deviation appears to occur in the family, although with no clinical significance.

Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 18 , Issue 1 , January 1969 , pp. 92 - 98
Copyright
Copyright © The International Society for Twin Studies 1969

References

Literatur

Chandra, H. S., Hungerford, D. A. (1963). An aberrant autosome (13-15) in a human female and her father, both apparently normal. Cytogenetics, 2: 34–41.CrossRefGoogle Scholar
Cooper, L. H., Hirschhorn, K. (1962). Enlarged satellites as a familial chromosome marker. Amer. J. Hum. Genet., 14: 107–124.Google ScholarPubMed
Court Brown, W. M., Jacobs, P. A., Brunton, M. (1965). Chromosome studies on randomly chosen men and women. Lancet, 2: 561.CrossRefGoogle Scholar
Court Brown, W. M., Buckton, K. E., Jacobs, P. A., Tough, J. M., Kuensberg, E. V., Knox, J. D. E. (1966). Chromosome Studies on Adults. Cambridge University Press, London.Google Scholar
Genest, P., Bourchard, M, Bourchard, J. (1967). Satellited human Y-chromosome. Lancet, 1: 1279–1280.CrossRefGoogle Scholar
Schade, H. (1963). Chromosomenanomalien beim Menschen. Med. Welt, 1: 2436–2442.Google Scholar
McKusick, V. A. (1960). Chromosomes in Marfan's disease. Lancet, 1: 1194.CrossRefGoogle Scholar
Starkmann, N. M., Shaw, W. M. (1967). Atypical acrocentric chromosomes in negro and Caucasians mongols. Amer. J. Hum. Genet., 19: 162–173.Google Scholar
Tjio, J. H., Puck, T. T., Robinson, A. (1960). The human chromosomal satellites in normal persons and in two patients with Marfan's syndrome. Proc. Nat. Acad. Sci., 46: 532–539.CrossRefGoogle ScholarPubMed