Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2003-6-3
pubmed:abstractText
The genetic basis of schizophrenia is obscure. In an XX male patient with schizophrenia we previously showed that one X;Y translocation breakpoint was in pseudoautosomal region 1 (PAR1) with the effect that the proximal segment of PAR1 from the PAR1 boundary to acetylserotonin N-methyl transferase (ASMT) distally was triplicated in this patient. This study determined whether dosage imbalances of X-Y homologous regions in general are associated with schizophrenia.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0955-8829
pubmed:author
pubmed:issnType
Print
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
115-9
pubmed:dateRevised
2010-9-1
pubmed:meshHeading
pubmed:year
2003
pubmed:articleTitle
Quantitation of X-Y homologous genes in patients with schizophrenia by multiplex polymerase chain reaction.
pubmed:affiliation
University of Oxford, Department of Psychiatry, Warneford Hospital, Oxford, UK. norman.ross@psychiatry.ox.ac.uk
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't