Skip to main content
  • 91 Accesses

Abstract

Chromosomal anomalies in human beings unhappily produce not only somatic disturbances, but also severe mental damage. Data have been accumulated on many different syndromes, permitting a general discussion of the mechanism by which such effects occur.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Lejeune, J., Gautier, M., and Turpin, R.: Les chromosomes humains en culture de tissus, C. R. Acad. Sci. Paris 248: 602–603, 1959.

    CAS  Google Scholar 

  2. Edwards, J.H., Harnden, D.G., Cameron, A.H., Grosse, V. M., and Wolff, O.H.: A new trisomic syndrome, Lancet 1: 787–789, 1960.

    Article  PubMed  CAS  Google Scholar 

  3. Patau, K., Smith, D. W., Therman, E., Inhorn, S. L., and Wagner, H. P.: Multiple congenital anomaly caused by an extra autosome, Lancet 1: 790–793, 1960.

    Article  PubMed  CAS  Google Scholar 

  4. Lyon, M. F.: Sex chromatin and gene action in the mammalian X chromosome, Am. J. Hum. Genet. 14: 135–148, 1962.

    PubMed  CAS  Google Scholar 

  5. Ford, C. E., Jones, K. W., Polani, P.E., de Almeida, J.C., and Briggs, J.H.: A sex chromosome anomaly in a case of gonadal dysgenesis (Turner’s syndrome), Lancet 1: 711–713, 1959.

    Article  PubMed  CAS  Google Scholar 

  6. Money, J. and Alexander, D.: Turner’s syndrome: Further demonstration of the presence of specific cognitional deficiencies, J. Med. Genet. 3: 47, 1966.

    Article  PubMed  CAS  Google Scholar 

  7. Jacobs, P.A., and Strong, J. A.: A case of human intersexuality having a possible XXY sex-determining mechanism, Nature 183: 302–303, 1959.

    Article  PubMed  CAS  Google Scholar 

  8. Jacobs, P. A., Brunton, M., Melville, M. E., Brittain, R. P., and McClemont, W. F.: Aggressive behaviour, mental subnormality and the XYY male, Nature 208: 1351, 1965.

    Article  PubMed  CAS  Google Scholar 

  9. Lejeune, R., Lafourcade, J., Berger, R., Vialatte, J., Boeswillwald, M., Seringe, P., and Turpin, R.: Trois cas de délétion partielle du bras court d’un chromosome 5, C.R. Acad. Sci. Paris 257: 3098–3102, 1963.

    PubMed  CAS  Google Scholar 

  10. Lejeune, J., Lafourcade, J., Berger, R., and Turpin, R.: Ségrégation familiale d’une translocation 5–13 déterminant une monosomie et une trisomie partielles du bras court du chromosome 5: Maladie du “cri du chat ° et sa *réciproque, ” C.R. Acad. Sci. Paris 258: 5767–5770, 1964.

    PubMed  CAS  Google Scholar 

  11. Lejeune, J., Berger, R., Réthoré, M.O., Archambault, L., Jerome, H., Thieffry, S., Aicardi, J., Broyer, M., Lafourcade, J., Cruveillier, J., and Turpin, R.: Monosomie partielle pour un petit acrocentrique, C.R. Acad. Sci. Paris 259: 4187–4190, 1964.

    PubMed  CAS  Google Scholar 

  12. Reisman, L.I., Kashara, S., Chung, C. Y., Darnell, A., and Hall, B.: Antimongolism. Studies in an infant with a partial monosomy of the 21 chromosome, Lancet 1: 394–397, 1966.

    Article  PubMed  CAS  Google Scholar 

  13. German, J., and Bearn, A.G., cited by Penrose, L.S.: Antimongolism, Lancet 1: 497, 1966.

    Google Scholar 

  14. deGrouchy, J., Royer, P., Salmon, C., and Lamy, M.: Délétion partielle des bras longs du chromosome 18, Path. et Biol. 12: 579, 1966.

    Google Scholar 

  15. Lejeune, J., Berger, R., Lafourcade, J., and Réthoré, M.O.: La délétion partielle du bras long du chromosome 18. Individualisation d’un nouvel état morbide, Ann. Genet. Paris 9: 32–38, 1966.

    PubMed  CAS  Google Scholar 

  16. deGrouchy, J., Lamy, M., Thieffry, S., Arthuis, M., and Salmon, C.: Dysmorphie complexe avec oligophrénie: Délétion des bras courts d’un chromosome 17–18, C.R. Acad. Sci. Paris 256: 1028–1029.

    Google Scholar 

  17. deGrouchy, J., Bonnette, J., and Salmon, C.: Délétion du bras court du chromosome 18, Ann. Genet. Paris 9: 19–26, 1966.

    PubMed  Google Scholar 

  18. Turpin, R., and Lejeune, J.: Les Chromosomes Humains, Gauthier-Villars, Edit., Paris, 1965.

    Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1967 Plenum Press

About this chapter

Cite this chapter

Lejeune, J. (1967). Chromosomal Studies in Psychiatry. In: Wortis, J. (eds) Recent Advances in Biological Psychiatry. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-8228-7_2

Download citation

  • DOI: https://doi.org/10.1007/978-1-4684-8228-7_2

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4684-8230-0

  • Online ISBN: 978-1-4684-8228-7

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics