| pubmed-article:11062837 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11062837 | lifeskim:mentions | umls-concept:C0007452 | lld:lifeskim |
| pubmed-article:11062837 | lifeskim:mentions | umls-concept:C1458140 | lld:lifeskim |
| pubmed-article:11062837 | lifeskim:mentions | umls-concept:C0728826 | lld:lifeskim |
| pubmed-article:11062837 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
| pubmed-article:11062837 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:11062837 | pubmed:dateCreated | 2000-12-12 | lld:pubmed |
| pubmed-article:11062837 | pubmed:abstractText | A study was designed to determine the inheritance pattern of a blood platelet aggregation disorder in Simmental cattle utilizing embryo transfer technology. A Simmental donor cow that had previously produced a calf with the platelet aggregation disorder was superovulated and mated to a bull that had also produced affected offspring. Twenty-seven calves were produced from the 63 (42.9%) embryos transferred. This somewhat lower than expected pregnancy rate is suggestive of an increased rate of embryo loss. Twenty-three of 25 (92%) calves had normal platelet aggregation patterns and 2 failed to show any evidence of platelet aggregation. Data are suggestive that inheritance is not simple Mendelian recessive. A more likely scenario is that the defect is the result of the inheritance of at least 2 genes, which is also consistent with the sporadic incidence reported in the population at large. | lld:pubmed |
| pubmed-article:11062837 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11062837 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11062837 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11062837 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11062837 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11062837 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11062837 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11062837 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11062837 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11062837 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11062837 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11062837 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11062837 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:11062837 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11062837 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:11062837 | pubmed:issn | 0008-5286 | lld:pubmed |
| pubmed-article:11062837 | pubmed:author | pubmed-author:SchmidtW KWK | lld:pubmed |
| pubmed-article:11062837 | pubmed:author | pubmed-author:SearcyG PGP | lld:pubmed |
| pubmed-article:11062837 | pubmed:author | pubmed-author:MapletoftR... | lld:pubmed |
| pubmed-article:11062837 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11062837 | pubmed:volume | 41 | lld:pubmed |
| pubmed-article:11062837 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11062837 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11062837 | pubmed:pagination | 791-3 | lld:pubmed |
| pubmed-article:11062837 | pubmed:dateRevised | 2010-9-14 | lld:pubmed |
| pubmed-article:11062837 | pubmed:meshHeading | pubmed-meshheading:11062837... | lld:pubmed |
| pubmed-article:11062837 | pubmed:meshHeading | pubmed-meshheading:11062837... | lld:pubmed |
| pubmed-article:11062837 | pubmed:meshHeading | pubmed-meshheading:11062837... | lld:pubmed |
| pubmed-article:11062837 | pubmed:meshHeading | pubmed-meshheading:11062837... | lld:pubmed |
| pubmed-article:11062837 | pubmed:meshHeading | pubmed-meshheading:11062837... | lld:pubmed |
| pubmed-article:11062837 | pubmed:meshHeading | pubmed-meshheading:11062837... | lld:pubmed |
| pubmed-article:11062837 | pubmed:meshHeading | pubmed-meshheading:11062837... | lld:pubmed |
| pubmed-article:11062837 | pubmed:meshHeading | pubmed-meshheading:11062837... | lld:pubmed |
| pubmed-article:11062837 | pubmed:meshHeading | pubmed-meshheading:11062837... | lld:pubmed |
| pubmed-article:11062837 | pubmed:year | 2000 | lld:pubmed |
| pubmed-article:11062837 | pubmed:articleTitle | A study of the inheritance of a bleeding disorder in Simmental cattle. | lld:pubmed |
| pubmed-article:11062837 | pubmed:affiliation | Department of Herd Medicine and Theriogenology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon. | lld:pubmed |
| pubmed-article:11062837 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11062837 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
