| pubmed-article:7279823 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:7279823 | lifeskim:mentions | umls-concept:C0241888 | lld:lifeskim |
| pubmed-article:7279823 | lifeskim:mentions | umls-concept:C0270952 | lld:lifeskim |
| pubmed-article:7279823 | lifeskim:mentions | umls-concept:C0332162 | lld:lifeskim |
| pubmed-article:7279823 | lifeskim:mentions | umls-concept:C0205087 | lld:lifeskim |
| pubmed-article:7279823 | pubmed:issue | 663 | lld:pubmed |
| pubmed-article:7279823 | pubmed:dateCreated | 1981-11-18 | lld:pubmed |
| pubmed-article:7279823 | pubmed:abstractText | An English family is described several members of which have suffered from oculopharyngeal muscular dystrophy. No symptoms were noticed in any affected members of the family until aged at least 50 years. An autosomal dominant pattern of inheritance is clearly shown. | lld:pubmed |
| pubmed-article:7279823 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7279823 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7279823 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7279823 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7279823 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7279823 | pubmed:language | eng | lld:pubmed |
| pubmed-article:7279823 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7279823 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:7279823 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7279823 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7279823 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:7279823 | pubmed:issn | 0032-5473 | lld:pubmed |
| pubmed-article:7279823 | pubmed:author | pubmed-author:KahnPP | lld:pubmed |
| pubmed-article:7279823 | pubmed:author | pubmed-author:IsenbergD ADA | lld:pubmed |
| pubmed-article:7279823 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7279823 | pubmed:volume | 57 | lld:pubmed |
| pubmed-article:7279823 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7279823 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7279823 | pubmed:pagination | 41-3 | lld:pubmed |
| pubmed-article:7279823 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:7279823 | pubmed:meshHeading | pubmed-meshheading:7279823-... | lld:pubmed |
| pubmed-article:7279823 | pubmed:meshHeading | pubmed-meshheading:7279823-... | lld:pubmed |
| pubmed-article:7279823 | pubmed:meshHeading | pubmed-meshheading:7279823-... | lld:pubmed |
| pubmed-article:7279823 | pubmed:meshHeading | pubmed-meshheading:7279823-... | lld:pubmed |
| pubmed-article:7279823 | pubmed:meshHeading | pubmed-meshheading:7279823-... | lld:pubmed |
| pubmed-article:7279823 | pubmed:meshHeading | pubmed-meshheading:7279823-... | lld:pubmed |
| pubmed-article:7279823 | pubmed:meshHeading | pubmed-meshheading:7279823-... | lld:pubmed |
| pubmed-article:7279823 | pubmed:meshHeading | pubmed-meshheading:7279823-... | lld:pubmed |
| pubmed-article:7279823 | pubmed:meshHeading | pubmed-meshheading:7279823-... | lld:pubmed |
| pubmed-article:7279823 | pubmed:meshHeading | pubmed-meshheading:7279823-... | lld:pubmed |
| pubmed-article:7279823 | pubmed:meshHeading | pubmed-meshheading:7279823-... | lld:pubmed |
| pubmed-article:7279823 | pubmed:year | 1981 | lld:pubmed |
| pubmed-article:7279823 | pubmed:articleTitle | Familial late onset oculopharyngeal muscular dystrophy. | lld:pubmed |
| pubmed-article:7279823 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:7279823 | pubmed:publicationType | Case Reports | lld:pubmed |
