Hereditary meningoencephalocele in Burmese cats
A syndrome of meningoencephalocele and related craniofacial abnormalities occurred in 19 (6 male, 3 female, 10 of unknown sex) of 88 kittens in 22 litters born to matings between Burmese cats that were known to produce this defect. This is consistent with the action of an autosomal recessive gene. T...
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Veröffentlicht in: | The Journal of heredity 1986-01, Vol.77 (1), p.60-60 |
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creator | Sponenberg, D.P. Graf-Webster, E. |
description | A syndrome of meningoencephalocele and related craniofacial abnormalities occurred in 19 (6 male, 3 female, 10 of unknown sex) of 88 kittens in 22 litters born to matings between Burmese cats that were known to produce this defect. This is consistent with the action of an autosomal recessive gene. The exceptional breeding record of one cat indicates that perhaps the phenotype is impenetrant in at least some homozygotes. The gene symbol mc is proposed for this defect. |
doi_str_mv | 10.1093/oxfordjournals.jhered.a110173 |
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This is consistent with the action of an autosomal recessive gene. The exceptional breeding record of one cat indicates that perhaps the phenotype is impenetrant in at least some homozygotes. The gene symbol mc is proposed for this defect.</description><identifier>ISSN: 0022-1503</identifier><identifier>EISSN: 1465-7333</identifier><identifier>DOI: 10.1093/oxfordjournals.jhered.a110173</identifier><identifier>PMID: 2937834</identifier><identifier>CODEN: JOHEA8</identifier><language>eng</language><publisher>Cary, NC: Oxford University Press</publisher><subject>Animals ; Biological and medical sciences ; Cat Diseases - genetics ; Cats ; Classical genetics, quantitative genetics, hybrids ; Crosses, Genetic ; Encephalocele - genetics ; Encephalocele - veterinary ; Female ; Fundamental and applied biological sciences. Psychology ; Genetics of eukaryotes. 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This is consistent with the action of an autosomal recessive gene. The exceptional breeding record of one cat indicates that perhaps the phenotype is impenetrant in at least some homozygotes. The gene symbol mc is proposed for this defect.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cat Diseases - genetics</subject><subject>Cats</subject><subject>Classical genetics, quantitative genetics, hybrids</subject><subject>Crosses, Genetic</subject><subject>Encephalocele - genetics</subject><subject>Encephalocele - veterinary</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Male</subject><subject>Meningocele - genetics</subject><subject>Meningocele - veterinary</subject><subject>Myanmar</subject><subject>Vertebrata</subject><issn>0022-1503</issn><issn>1465-7333</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1v1DAQhi1EVbaFn4C0B-CW7UwcZ-wDB6hoF6lVKxUk1IvldSY0Sz62diKVf19XGyr1xMmS3-f1jB8hPiKsEIw8GR7qIVTbYQq9a-Nqe8eBq5VDBCT5SiywKFVGUsrXYgGQ5xkqkG_EUYxbAEBl4FAc5kaSlsVCnKyf6s3owt9lx33T_x6497y7c-3gueVl0y-_TqHjyEvvxvhWHNRpLL-bz2Px8-zbj9N1dnF1_v30y0XmC9RjRhp8rY2TqqK6YlWBqXRuNoTAmsARG-9l7WBTVBWj1lqC06QQkUrQRh6LT_t3d2G4nziOtmtiWqh1PQ9TtFRSqUpD_wWxIDJ5qRP4eQ_6MMQYuLa70HTp3xbBPpm1L83avVk7m0399_OgadOl-3_tWWXKP8y5i961dXC9b-IzppVOK-cJy_ZYE0d-eI5d-GNLkqTs-tetvb65vT67xHN7Ix8BqGOX4g</recordid><startdate>198601</startdate><enddate>198601</enddate><creator>Sponenberg, D.P.</creator><creator>Graf-Webster, E.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>198601</creationdate><title>Hereditary meningoencephalocele in Burmese cats</title><author>Sponenberg, D.P. ; Graf-Webster, E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-780cf89a35d7fde5d09d829b710e870a7e9cc3fa0b4dde188830a875111760893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cat Diseases - genetics</topic><topic>Cats</topic><topic>Classical genetics, quantitative genetics, hybrids</topic><topic>Crosses, Genetic</topic><topic>Encephalocele - genetics</topic><topic>Encephalocele - veterinary</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Male</topic><topic>Meningocele - genetics</topic><topic>Meningocele - veterinary</topic><topic>Myanmar</topic><topic>Vertebrata</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sponenberg, D.P.</creatorcontrib><creatorcontrib>Graf-Webster, E.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of heredity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sponenberg, D.P.</au><au>Graf-Webster, E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hereditary meningoencephalocele in Burmese cats</atitle><jtitle>The Journal of heredity</jtitle><addtitle>J Hered</addtitle><date>1986-01</date><risdate>1986</risdate><volume>77</volume><issue>1</issue><spage>60</spage><epage>60</epage><pages>60-60</pages><issn>0022-1503</issn><eissn>1465-7333</eissn><coden>JOHEA8</coden><abstract>A syndrome of meningoencephalocele and related craniofacial abnormalities occurred in 19 (6 male, 3 female, 10 of unknown sex) of 88 kittens in 22 litters born to matings between Burmese cats that were known to produce this defect. This is consistent with the action of an autosomal recessive gene. The exceptional breeding record of one cat indicates that perhaps the phenotype is impenetrant in at least some homozygotes. The gene symbol mc is proposed for this defect.</abstract><cop>Cary, NC</cop><pub>Oxford University Press</pub><pmid>2937834</pmid><doi>10.1093/oxfordjournals.jhered.a110173</doi><tpages>1</tpages></addata></record> |
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source | MEDLINE; Oxford University Press Journals Digital Archive Legacy |
subjects | Animals Biological and medical sciences Cat Diseases - genetics Cats Classical genetics, quantitative genetics, hybrids Crosses, Genetic Encephalocele - genetics Encephalocele - veterinary Female Fundamental and applied biological sciences. Psychology Genetics of eukaryotes. Biological and molecular evolution Male Meningocele - genetics Meningocele - veterinary Myanmar Vertebrata |
title | Hereditary meningoencephalocele in Burmese cats |
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