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pubmed-article:12782970pubmed:abstractTextThe 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.lld:pubmed
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pubmed-article:12782970pubmed:articleTitleQuantitation of X-Y homologous genes in patients with schizophrenia by multiplex polymerase chain reaction.lld:pubmed
pubmed-article:12782970pubmed:affiliationUniversity of Oxford, Department of Psychiatry, Warneford Hospital, Oxford, UK. norman.ross@psychiatry.ox.ac.uklld:pubmed
pubmed-article:12782970pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12782970pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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