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Marker chromosomes in parents of spontaneous abortuses

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Summary

In a study of spontaneous abortuses, the karyotype of 80 parental pairs were investigated in detail for chromosomal markers using Quinacrine-stained chromosome preparations from cultures of peripheral blood. Chromosomal markers were found in 26.9% of the parents and there was no difference between the frequency among parents of chromosomally abnormal and chromosomally normal abortuses.

Grouping of the markers in p+ or s+ and qh+ variants showed that there was a statistically significant difference between parents with karyotypically normal and abnormal abortuses, p+ and s+ variants being more frequent in the first and qh+ more frequent in the second group.

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References

  • Court Brown, W. M., Buckton, K. E., Jacobs, P. A., Tough, J. M., Kuenssberg, E. V., Knox, J. D.: Chromosome studies on adults. Eugenics Laboratory Memoirs 42, London 1966

  • Dekaban, A. S., Bender, M. A., Economos, G. E.: Chromosome studies in mongoloids and their families. Cytogenetics 2, 61–75 (1963)

    Google Scholar 

  • Grouchy, J. de, Thieffry, S., Arthuis, M., Gerbeaux, J., Poupinet, S., Salmon, Ch., Lamy, M.: Chromosomes marqueurs familiaux et aneuploidie. Rôle possible de l'interaction chromosomique. Ann. Génét. 7, 76–83 (1964)

    Google Scholar 

  • Hamerton, J. L.: Human cytogenetics. General cytogenetics, Vol. I. New York-London: Academic Press 1971

    Google Scholar 

  • Hamerton, J. L., Giannelli, F., Polani, P. E.: Cytogenetics of Down's syndrome (mongolism). I. Data on a consecutive series of patients referred for genetic counselling and diagnosis. Cytogenetics 4, 171–185 (1965)

    Google Scholar 

  • Hamerton, J. L., Ray, M., Abbot, J., Williamson, Ch., Ducasse, G. C.: Chromosome studies in a neonatal population. Canad. med. Ass. J. 106, 776–779 (1972)

    Google Scholar 

  • Jones, K. W., Corneo, G.: Location of satellite and homogenous DNA sequences on human chromosomes. Nature (Lond.) New Biol. 233, 268–271 (1971)

    Google Scholar 

  • Jones, K. W., Prosser, J., Corneo, G., Ginelli, E.: The chromosomal location of human satellite DNA III. Chromosoma (Berl.) 42, 445–451 (1973)

    Google Scholar 

  • Lubs, H. A., Ruddle, F. H.: Applications of quantitative karyotypy to chromosome variation in 4400 consecutive newborns. Human Population Cytogenetics. Pfizer Medical Monographs 5. Edinburgh U/P 1970

  • Lubs, H. A., McKenzie, W. H., Patil, S. R., Merrick, S.: New staining methods for chromosomes. Methods in cell biology, Vol. VI. New York-London: Academic Press 1973

    Google Scholar 

  • Mikelsaar, A.-V. N., Tüür, S. J., Käosaar, M. E.: Human karyotype polymorphism I. Routine and flourescence investigation of chromosomes in a normal adult population. Humangenetik 20, 89–101 (1973)

    Google Scholar 

  • Nielsen, J., Friedrich, U.: Length of the Y chromosome in criminal males. Clin. Genet. 3, 281–285 (1972)

    Google Scholar 

  • Nielsen, J., Friedrich, U., Hreidarsson, A. B., Zeuthen, E.: Frequency of 9 qh+ and risk of chromosome aberrations in the progeny of individuals with 9 qh+. Humangenetik (in prep.)

  • Sands, V. E.: Short arm enlargement in acrocentric chromosomes. Amer. J. hum. Genet. 21, 293–304 (1969)

    Google Scholar 

  • Šubrt, J.: A further example of familial Gp+ associated with trisomy C. Humangenetik 9, 86–90 (1970)

    Google Scholar 

  • Therkelsen, A. J.: Enlarged short arm of a small acrocentric chromosome in grandfather, mother and child, the latter with Down's syndrome. Cytogenetics 3, 441–451 (1964)

    Google Scholar 

  • Therkelsen, A. J., Grunnet, N., Hjort, T., Jensen, O. M., Jonasson, J., Lauritsen, J. G., Lindsten, J., Petersen, G. B.: Studies on spontaneous abortions. Proceedings of the Symposium on chromosomal errors in relation to reproductive failure. Paris (1973)

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Holbek, S., Friedrich, U., Lauritsen, J.G. et al. Marker chromosomes in parents of spontaneous abortuses. Hum Genet 25, 61–64 (1974). https://doi.org/10.1007/BF00281007

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