{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,5]],"date-time":"2026-05-05T03:10:13Z","timestamp":1777950613795,"version":"3.51.4"},"reference-count":8,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2012,7,4]],"date-time":"2012-07-04T00:00:00Z","timestamp":1341360000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Animal Genetics"],"published-print":{"date-parts":[[2013,4]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>A genome scan was conducted to map the autosomal recessive lethal disorder brachygnathia, cardiomegaly and renal hypoplasia syndrome (<jats:styled-content style=\"fixed-case\">BCRHS<\/jats:styled-content>) in <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>oll <jats:styled-content style=\"fixed-case\">M<\/jats:styled-content>erino sheep. The scan involved 10 affected and 27 unaffected animals from a single <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>oll <jats:styled-content style=\"fixed-case\">M<\/jats:styled-content>erino\/<jats:styled-content style=\"fixed-case\">M<\/jats:styled-content>erino sheep flock, which were genotyped with the <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>llumina <jats:styled-content style=\"fixed-case\">O<\/jats:styled-content>vine <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>50 <jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>ead<jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>hip. Association and homozygosity mapping analyses located the disorder in a region comprising 20 consecutive <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s spanning 1.1\u00a0Mb towards the distal end of chromosome <jats:styled-content style=\"fixed-case\">OAR<\/jats:styled-content>2. All affected animals and none of the unaffected animals were homozygous for the associated haplotype in this region. These results provide the basis for identifying the causative mutation(s) and should enable the development of a <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> test to identify carriers in the Poll Merino sheep population. Understanding the molecular control of <jats:styled-content style=\"fixed-case\">BCRHS<\/jats:styled-content> may provide insight into the fundamental genetic control and regulation of the affected organ systems.<\/jats:p>","DOI":"10.1111\/j.1365-2052.2012.02392.x","type":"journal-article","created":{"date-parts":[[2012,7,5]],"date-time":"2012-07-05T07:55:12Z","timestamp":1341474912000},"page":"231-233","source":"Crossref","is-referenced-by-count":12,"title":["Brachygnathia, cardiomegaly and renal hypoplasia syndrome (<scp>BCRHS<\/scp>) in <scp>M<\/scp>erino sheep maps to a 1.1\u2010megabase region on ovine chromosome <scp>OAR<\/scp>2"],"prefix":"10.1111","volume":"44","author":[{"given":"M. R.","family":"Shariflou","sequence":"first","affiliation":[{"name":"Faculty of Veterinary Science University of Sydney Sydney NSW 2006 Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C. 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