Triplication of several PAR1 genes and part of the Homo sapiens specific Yp11.2/Xq21.3 region of homology in a 46,X, t(X;Y) (p22.33;p11.2) male with schizophrenia
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| Veröffentlicht in: | Journal of medical genetics 2001-10, Vol.38 (10), p.710-719 |
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| container_issue | 10 |
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| container_title | Journal of medical genetics |
| container_volume | 38 |
| creator | ROSS, Norman L. J JIAN YANG SARGENT, Carole A BOUCHER, Catherine A NANKO, Shinichiro WADEKAR, Rekha WILLIAMS, Nic A AFFARA, Nabeel A CROW, Timothy J |
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| doi_str_mv | 10.1136/jmg.38.10.710 |
| format | Article |
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Psychiatry ; Psychoses ; Radiation Hybrid Mapping ; Restriction Mapping ; Schizophrenia ; Schizophrenia - complications ; Schizophrenia - genetics ; Sequence Homology, Nucleic Acid ; Sequence Tagged Sites ; Sex Chromosome Disorders - complications ; Sex Chromosome Disorders - genetics ; Translocation, Genetic - genetics ; X Chromosome - genetics ; Y Chromosome - genetics</subject><ispartof>Journal of medical genetics, 2001-10, Vol.38 (10), p.710-719</ispartof><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c382t-54d540fc0eed718d5bd8ed0aec9657923225536d5c30626df0e8ab73da4241263</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1734742/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1734742/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14147861$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11594342$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ROSS, Norman L. J</creatorcontrib><creatorcontrib>JIAN YANG</creatorcontrib><creatorcontrib>SARGENT, Carole A</creatorcontrib><creatorcontrib>BOUCHER, Catherine A</creatorcontrib><creatorcontrib>NANKO, Shinichiro</creatorcontrib><creatorcontrib>WADEKAR, Rekha</creatorcontrib><creatorcontrib>WILLIAMS, Nic A</creatorcontrib><creatorcontrib>AFFARA, Nabeel A</creatorcontrib><creatorcontrib>CROW, Timothy J</creatorcontrib><title>Triplication of several PAR1 genes and part of the Homo sapiens specific Yp11.2/Xq21.3 region of homology in a 46,X, t(X;Y) (p22.33;p11.2) male with schizophrenia</title><title>Journal of medical genetics</title><addtitle>J Med Genet</addtitle><subject>Adult and adolescent clinical studies</subject><subject>Asian Continental Ancestry Group - genetics</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Cell Line, Transformed</subject><subject>Chromosome Breakage - genetics</subject><subject>Cloning, Molecular</subject><subject>Gene Amplification - genetics</subject><subject>Genes, Duplicate - genetics</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Japan</subject><subject>Letters to the Editor</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microsatellite Repeats - genetics</subject><subject>Molecular Sequence Data</subject><subject>Polymerase Chain Reaction</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychoses</subject><subject>Radiation Hybrid Mapping</subject><subject>Restriction Mapping</subject><subject>Schizophrenia</subject><subject>Schizophrenia - complications</subject><subject>Schizophrenia - genetics</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Sequence Tagged Sites</subject><subject>Sex Chromosome Disorders - complications</subject><subject>Sex Chromosome Disorders - genetics</subject><subject>Translocation, Genetic - genetics</subject><subject>X Chromosome - genetics</subject><subject>Y Chromosome - genetics</subject><issn>0022-2593</issn><issn>1468-6244</issn><issn>1468-6244</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkV9L3UAQxZdSqbfax76WeSkomLizu9nkIhREbC0ILWLh-hT27k6SlfxzN7Xox-knba5eavs0HOZ3zsAcxt4jTxGlPr7t6lQW6Sxz5K_YApUuEi2Ues0WnAuRiGwpd9nbGG85R5mjfsN2EbOlkkos2O_r4MfWWzP5oYehgkj3FEwL30-vEGrqKYLpHYwmTJv11BBcDN0A0Yye-ghxJOsrb-FmREzF8epOYCohUL0NbGa6HeoH8D0YUPpodQTTwerk5hAORiFSKU-enIfQmZbgl58aiLbxj8PYBOq92Wc7lWkjvdvOPfbj8_n12UVy-e3L17PTy8TKQkxJplymeGU5kcuxcNnaFeS4IbvUWb4UUogsk9plVnIttKs4FWadS2eUUCi03GOfnnPHn-uOnKV-mh9RjsF3JjyUg_Hl_5veN2U93JeYS5UrMQckzwE2DDEGqv56kZebssq5rFIWGzmXNfMf_j34Qm_bmYGPW8BEa9oqmN76-MIpVHmhUf4BosybRw</recordid><startdate>20011001</startdate><enddate>20011001</enddate><creator>ROSS, Norman L. 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J ; JIAN YANG ; SARGENT, Carole A ; BOUCHER, Catherine A ; NANKO, Shinichiro ; WADEKAR, Rekha ; WILLIAMS, Nic A ; AFFARA, Nabeel A ; CROW, Timothy J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-54d540fc0eed718d5bd8ed0aec9657923225536d5c30626df0e8ab73da4241263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult and adolescent clinical studies</topic><topic>Asian Continental Ancestry Group - genetics</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Cell Line, Transformed</topic><topic>Chromosome Breakage - genetics</topic><topic>Cloning, Molecular</topic><topic>Gene Amplification - genetics</topic><topic>Genes, Duplicate - genetics</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Japan</topic><topic>Letters to the Editor</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microsatellite Repeats - genetics</topic><topic>Molecular Sequence Data</topic><topic>Polymerase Chain Reaction</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>Radiation Hybrid Mapping</topic><topic>Restriction Mapping</topic><topic>Schizophrenia</topic><topic>Schizophrenia - complications</topic><topic>Schizophrenia - genetics</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Sequence Tagged Sites</topic><topic>Sex Chromosome Disorders - complications</topic><topic>Sex Chromosome Disorders - genetics</topic><topic>Translocation, Genetic - genetics</topic><topic>X Chromosome - genetics</topic><topic>Y Chromosome - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ROSS, Norman L. 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| ispartof | Journal of medical genetics, 2001-10, Vol.38 (10), p.710-719 |
| issn | 0022-2593 1468-6244 1468-6244 |
| language | eng |
| recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1734742 |
| source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection |
| subjects | Adult and adolescent clinical studies Asian Continental Ancestry Group - genetics Base Sequence Biological and medical sciences Cell Line, Transformed Chromosome Breakage - genetics Cloning, Molecular Gene Amplification - genetics Genes, Duplicate - genetics Humans In Situ Hybridization, Fluorescence Japan Letters to the Editor Male Medical sciences Microsatellite Repeats - genetics Molecular Sequence Data Polymerase Chain Reaction Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychoses Radiation Hybrid Mapping Restriction Mapping Schizophrenia Schizophrenia - complications Schizophrenia - genetics Sequence Homology, Nucleic Acid Sequence Tagged Sites Sex Chromosome Disorders - complications Sex Chromosome Disorders - genetics Translocation, Genetic - genetics X Chromosome - genetics Y Chromosome - genetics |
| title | Triplication of several PAR1 genes and part of the Homo sapiens specific Yp11.2/Xq21.3 region of homology in a 46,X, t(X;Y) (p22.33;p11.2) male with schizophrenia |
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