Skip to main content
SpringerLink
Log in

Brief report: Translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia

  • Brief Reports
  • Published:
Journal of Autism and Developmental Disorders Aims and scope Submit manuscript

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

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

References

  • Bassett, A. S., Jones, B. D., McGillivray, B. C., & Pantzar, J. T. (1988). Partial trisomy chromosome 5 cosegregating with schizophrenia.Lancet, 1, 799–801.

    Google Scholar 

  • Bassett, A. (1992). Chromosomal abnormalities and schizophrenia.British Journal of Psychiatry, 161, 223–234.

    Google Scholar 

  • Bassett, A. S. (1991). Linkage analysis of schizophrenia: challenges and promise.Social Biology, 38, 189–196.

    Google Scholar 

  • Campion, D., D'Amato, T., Laklou, H., Sabate, O., Jay, M., Leboyer, M., Malafosse, A., Gorwood, P., Babron, M.C., Hillaire, D., Clerget-Darpoux, F., Waksman, G., & Mallet, J. (1992). Failure to replicate linkage between chromosome 5q11–q13 markers and schizophrenia in 28 families.Psychiatry Research, 44, 171–179.

    Google Scholar 

  • Childs, B., & Scriver, C. (1986). Age at onset and causes of disease.Perspectives in Biology and Medicine, 29, 437–460.

    Google Scholar 

  • DeLisi, L. E., Reiss, A. L., White, B. J., & Gershon, E. S. (1988). Cytogenetic studies of males with schizophrenia. Screening for the fragile X chromosome and other chromosomal abnormalities.Schizophrenia Research, 1, 277–281.

    Google Scholar 

  • Fish, B. (1977). Neurobiological antecedents of schizophrenia in children: Evidence for an inherited, congenital, neurointegrative defect.Archives of General Psychiatry, 34, 1297–1313.

    Google Scholar 

  • Fish, B. (1992). Infants at risk for schizophrenia: sequelae of a genetic neurointegrative defect.Archives of General Psychiatry, 49, 221–235.

    Google Scholar 

  • Fletcher, J., Evans, K., Baillie, D., Byrd, P., Hanratty, D., Leach, S., Julier, C., Gosden, J. R., Muir, W., Porteous, D. J., St. Clair, D., & Van Heyningen, V. (1993). Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources.American Journal of Human Genetics, 52, 478–490.

    Google Scholar 

  • Frezal, J. (1987). Genes, gene map, gene mapping.Cytogenetics and Cell Genetics, 46, 1–8.

    Google Scholar 

  • Gordon, C. T., McKenna, K., Giedd, J., Zametkin, A., Zahn, T., Hong, W., Kaysen, D., & Rapoport, J. (in press). Childhood onset schizophrenia: Neurobiologic characterization and pharmacologic response: NIMH studies in progress.Schizophrenia Bulletin.

  • Gottesman, I. (1991).Schizophrenia genesis: The origins of madness. San Francisco: W.H. Freeman.

    Google Scholar 

  • Kaplan, A. (1970). Chromosomal mosaicisms and occasional acentric chromosomal fragments in schizophrenic patients.Biological Psychiatry, 21, 89–94.

    Google Scholar 

  • Lopreiato, J. O., & Wulfsberg, E. A. (1992). A complex chromosome rearrangement in a boy with autism.Journal of Developmental and Behavioral Pediatrics, 13, 281–283.

    Google Scholar 

  • McGue, M., & Gottesman, I. I. (1991). The genetic epidemiology of schizophrenia and the design of linkage studies.European Archives of Psychiatry and Clinical Neuroscience, 240, 174–181.

    Google Scholar 

  • McGuffin, P., & Murray, R. (Eds.). (1991).The new genetics of mental illness. London: Butterworth-Heineman.

    Google Scholar 

  • Muir, W., Blackwood, D., St. Clair, D., Walker, M., Baillie, D., & Hubbard, A. (1991). Linkage analysis of schizophrenia with polymorphic loci on chromosome 11q.Cytogenetics and Cell Genetics, 58, 1966.

    Google Scholar 

  • Orkin, S. (1986). Reverse genetics and human disease.Cell, 47, 845–850.

    Google Scholar 

  • Petty, L. K., Ornitz, E. M., Michelman, J. D., & Zimmerman, E. G. (1984). Autistic children who become schizophrenic.Archives of General Psychiatry, 41, 129–135.

    Google Scholar 

  • Ramos-Arroyo, M. A., Rodriguez-Pinilla, E., & Cordera, J. F. (1992). Maternal diabetes: the risk for specific birth defects.European Journal of Epidemiology, 8, 503–508.

    Google Scholar 

  • Russell, A. T., Bott, L., & Sammons, C. (1989). The phenomenology of schizophrenia occurring in childhood.Journal of the American Academy of Child and Adolescent Psychiatry, 28, 399–407.

    Google Scholar 

  • Schinzel, A. (1988). Microdeletion syndromes, balanced translocations, and gene mapping.Journal of Medical Genetics, 25, 454–462.

    Google Scholar 

  • Slater, E., & Cowie, V. (1971).The genetics of mental disorders. London: Oxford University Press.

    Google Scholar 

  • Smith, M., Wasmuth, J., McPherson, J. D., Wagner, C., Grandy, D., Civelli, O., Potkin, S., & Litt, M. (1989). Cosegregation of an 11q22.3-9p22 translocation with affective disorder: proximity of the dopamine D2 receptor gene relative to the translocation breakpoint.American Journal of Human Genetics, 45, A220.

    Google Scholar 

  • Spitzer, R., & Endicott, J. (1978).Schedule for affective disorders and schizophrenia (3rd ed.). New York: Biometrics Research Division, New York State Psychiatric Institute.

    Google Scholar 

  • Su, Y., Burke, J., O'Neill, F. A., Murphy, B., Nie, L., Kipps, B., Bray, J., Shinkwin, R., Ni Nuallain, M., MacLean, C. J., Walsh, D., Diehl, S. R., & Kendler, K. S. (1993). Exclusion of linkage between schizophrenia and the D2 Dopamine receptor gene region of chromosome 11q in 112 Irish multiplex families.Archives of General Psychiatry, 50, 205–211.

    Google Scholar 

  • Sutherland, G. R. (1977). Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium.Science, 197, 265–266.

    Google Scholar 

  • Volkmar, F. R., & Cohen, D. J. (1991). Comorbid association of autism and schizophrenia.American Journal of Psychiatry, 148, 1705.

    Google Scholar 

  • Volkmar, F. R., Cohen, D., Hoshino, V., Rende, R., & Paul, R. (1988). Phenomenology and classification of the childhood psychoses.Psychological Medicine 18, 191–201.

    Google Scholar 

  • Walker, E., & Lewine, R. J. (1990). Predication of adult-onset schizophrenia from childhood home movies of the patients.American Journal of Psychiatry, 147, 1052–1056.

    Google Scholar 

  • Wang, Z. W., Black, D., Andreasen, N., & Crowe, R. (1993a). Pseudoautosomal locus for schizophrenia excluded in 12 pedigrees.Archives of General Psychiatry, 50, 199–204.

    Google Scholar 

  • Wang, Z. W., Black, D., Andreasen, N. C., & Crowe, R. R. (1993b). A linkage study of chromosome 11q in schizophrenia.Archives of General Psychiatry, 50, 212–216.

    Google Scholar 

  • Watkins, J., Asarnow, R., & Tanguay, P. (1988). Symptom development in childhood onset schizophrenia.Journal of Child Psychology and Psychiatry, 29, 865–878.

    Google Scholar 

  • Yunis, J. J. (1976). High resolution of human chromosomes.Science, 191, 1268–1270.

    Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Child Psychiatry Branch, National Institute of Mental Health, Building 10, Room 6N240, 9000 Rockville Pike, 20892, Bethesda, Maryland

    Charles T. Gordon, Marge Lenane & Judith L. Rapoport

  2. Human Genetics Branch, National Institutes of Health, USA

    Donna Krasnewich

  3. Cytogenetics Unit, Laboratory of Chemical Biology, National Institute of Diabetes, Digestive and Kidney Diseases, USA

    Beverly White

Authors
  1. Charles T. Gordon
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Donna Krasnewich
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Beverly White
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Marge Lenane
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Judith L. Rapoport
    View author publications

    You can also search for this author in PubMed Google Scholar

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gordon, C.T., Krasnewich, D., White, B. et al. Brief report: Translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia. J Autism Dev Disord 24, 537–545 (1994). https://doi.org/10.1007/BF02172134

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02172134

Keywords

Search

Navigation