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Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11

Authors :
Karayiorgou, Maria
Morris, Michael A.
Morrow, Bernice
Shprintzen, Robert J.
Goldberg, Rosalie
Borrow, Julian
Gos, Arnaud
Nestadt, Gerald
Wolyniec, Paula S.
Lasseter, Virginia K.
Eisen, Harvey
Childs, Barten
Kazazian, Haig H.
Kucherlapati, Raju
Antonarakis, Stylianos E.
Pulver, Ann E.
Housman, David E.
Source :
Proceedings of the National Academy of Sciences of the United States. August 15, 1995, Vol. 92 Issue 17, p7612, 5 p.
Publication Year :
1995

Abstract

The etiology of schizophrenia is thought to be both genetic and experiential. A genetic study of a group of schizophrenic patients shows two interstitial deletions on chromosome 22q11. The size of the deletions is calculated to be between 1.5 to 2 megabases. Another purpose of the study was to see if differences in deletion size were related to the schizophrenic phenotype in patients with velocardiofacial syndrome. Details of study on overlap between schizophrenia and velocardiofacial syndrome and the results are described.

Details

ISSN :
00278424
Volume :
92
Issue :
17
Database :
Gale General OneFile
Journal :
Proceedings of the National Academy of Sciences of the United States
Publication Type :
Academic Journal
Accession number :
edsgcl.17943895