Complex segregation analysis of Gilles de la Tourette syndrome: further evidence for a major locus mode of transmission
A sample of 35 published pedigrees of Gilles de la Tourette syndrome is studied using complex segregation analysis with pointers. Results indicate the presence of a rare, semidominant, incompletely penetrant allele leading to affection. This result is consistent with that previously reported by Comi...
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Veröffentlicht in: | American journal of human genetics 1984-05, Vol.36 (3), p.704-709 |
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description | A sample of 35 published pedigrees of Gilles de la Tourette syndrome is studied using complex segregation analysis with pointers. Results indicate the presence of a rare, semidominant, incompletely penetrant allele leading to affection. This result is consistent with that previously reported by Comings et al. on a larger, independent sample. |
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J</creator><creatorcontrib>DEVOR, E. J</creatorcontrib><description>A sample of 35 published pedigrees of Gilles de la Tourette syndrome is studied using complex segregation analysis with pointers. Results indicate the presence of a rare, semidominant, incompletely penetrant allele leading to affection. This result is consistent with that previously reported by Comings et al. on a larger, independent sample.</description><identifier>ISSN: 0002-9297</identifier><identifier>EISSN: 1537-6605</identifier><identifier>PMID: 6587775</identifier><identifier>CODEN: AJHGAG</identifier><language>eng</language><publisher>Chicago, IL: University of Chicago Press</publisher><subject>Alleles ; Biological and medical sciences ; Chromosome Mapping ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. 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J</creatorcontrib><title>Complex segregation analysis of Gilles de la Tourette syndrome: further evidence for a major locus mode of transmission</title><title>American journal of human genetics</title><addtitle>Am J Hum Genet</addtitle><description>A sample of 35 published pedigrees of Gilles de la Tourette syndrome is studied using complex segregation analysis with pointers. Results indicate the presence of a rare, semidominant, incompletely penetrant allele leading to affection. This result is consistent with that previously reported by Comings et al. on a larger, independent sample.</description><subject>Alleles</subject><subject>Biological and medical sciences</subject><subject>Chromosome Mapping</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Female</subject><subject>Genes</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Models, Genetic</subject><subject>Neurology</subject><subject>Pedigree</subject><subject>Probability</subject><subject>Tourette Syndrome - genetics</subject><issn>0002-9297</issn><issn>1537-6605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUcFKxDAQLaKs6-onCDmIt8I0aZvGgyCLroLgZT2XtJnsZkmbNWlX9-8NuCx68jQD782b92ZOkmlWMJ6WJRSnyRQAaCqo4OfJRQgbgCyrgE2SSVlUnPNimnzOXbe1-EUCrjyu5GBcT2Qv7T6YQJwmC2MtBqKQWEmWbvQ4DEjCvlfedXhH9OiHNXqCO6Owb5Fo54kkndzEal07BtK5OB2lBi_70JkQ4o7L5ExLG_DqUGfJ-9Pjcv6cvr4tXuYPr-mW0WxIMaOKM2RVkze8wkbyAnQOVEmtUAkOqi0Y4xxZwWM4CQwQY6s11Q0FwWbJ_Y_udmw6VC320YWtt9500u9rJ039F-nNul65XZ2VVZ4XEAVuDwLefYwYhjomaNFa2aMbQ11lIATn7F9ixgRwCnkkXv-2dPRy-EnEbw64DK20Ol6tNeFIq-I6ISj7BvEbmSI</recordid><startdate>19840501</startdate><enddate>19840501</enddate><creator>DEVOR, E. 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Prion diseases</topic><topic>Female</topic><topic>Genes</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Models, Genetic</topic><topic>Neurology</topic><topic>Pedigree</topic><topic>Probability</topic><topic>Tourette Syndrome - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DEVOR, E. 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J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complex segregation analysis of Gilles de la Tourette syndrome: further evidence for a major locus mode of transmission</atitle><jtitle>American journal of human genetics</jtitle><addtitle>Am J Hum Genet</addtitle><date>1984-05-01</date><risdate>1984</risdate><volume>36</volume><issue>3</issue><spage>704</spage><epage>709</epage><pages>704-709</pages><issn>0002-9297</issn><eissn>1537-6605</eissn><coden>AJHGAG</coden><abstract>A sample of 35 published pedigrees of Gilles de la Tourette syndrome is studied using complex segregation analysis with pointers. Results indicate the presence of a rare, semidominant, incompletely penetrant allele leading to affection. This result is consistent with that previously reported by Comings et al. on a larger, independent sample.</abstract><cop>Chicago, IL</cop><pub>University of Chicago Press</pub><pmid>6587775</pmid><tpages>6</tpages></addata></record> |
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subjects | Alleles Biological and medical sciences Chromosome Mapping Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Female Genes Humans Male Medical sciences Models, Genetic Neurology Pedigree Probability Tourette Syndrome - genetics |
title | Complex segregation analysis of Gilles de la Tourette syndrome: further evidence for a major locus mode of transmission |
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