Chromosomal abnormalities and schizophrenia
- 1 January 2000
- journal article
- review article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 97 (1) , 45-51
- https://doi.org/10.1002/(sici)1096-8628(200021)97:1<45::aid-ajmg6>3.0.co;2-9
Abstract
No abstract availableKeywords
This publication has 55 references indexed in Scilit:
- Chromosome 22 workshop reportAmerican Journal of Medical Genetics, 1999
- ‘Pfropfschizophrenie’ revisitedThe British Journal of Psychiatry, 1998
- Chromosome 22qll deletionsThe British Journal of Psychiatry, 1998
- Identification of an Interstitial Deletion in an Adult Female with Schizophrenia, Mental Retardation, and Dysmorphic Features: Further Support for a Putative Schizophrenia-Susceptibility Locus at 5q21-23.1American Journal of Human Genetics, 1997
- Support for a possible schizophrenia vulnerability locus in region 5q22–31 in Irish familiesMolecular Psychiatry, 1997
- Cytogenetic abnormalities on chromosome 18 associated with bipolar affective disorder or schizophreniaThe British Journal of Psychiatry, 1997
- Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein to 18q22.3American Journal of Medical Genetics, 1996
- Association of schizophrenia and partial trisomy of chromosome 5p: A case reportSchizophrenia Research, 1992
- The Association Between Triple X and PsychosisThe British Journal of Psychiatry, 1992
- Late‐Onset psychosis in the velo‐cardio‐facial syndromeAmerican Journal of Medical Genetics, 1992