| Literature DB >> 1677599 |
L E Delisi1, T J Crow, K E Davies, J D Terwilliger, J Ott, R Ram, T Flint, A Boccio.
Abstract
The hypothesis that at least a subgroup of familial cases of schizophrenia could be due to a genetic defect on the X chromosome is supported by the observation of an excess of X-chromosome aneuploidies (XXX and XXY) among populations of patients with psychosis. The distal long arm, Xq27-q28, is a candidate region where linkage has been claimed to manic-depressive disorder and a fragile site has been associated with schizophrenia spectrum disorders. The present study excluded linkage to a large part of this region using four polymorphic probes and multipoint lod-score analysis in 10 families with multiple members with schizophrenia.Entities:
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Year: 1991 PMID: 1677599 DOI: 10.1192/bjp.158.5.630
Source DB: PubMed Journal: Br J Psychiatry ISSN: 0007-1250 Impact factor: 9.319