pubmed-article:9158217 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:9158217 | lifeskim:mentions | umls-concept:C0015576 | lld:lifeskim |
pubmed-article:9158217 | lifeskim:mentions | umls-concept:C0337810 | lld:lifeskim |
pubmed-article:9158217 | lifeskim:mentions | umls-concept:C0085413 | lld:lifeskim |
pubmed-article:9158217 | lifeskim:mentions | umls-concept:C1418600 | lld:lifeskim |
pubmed-article:9158217 | lifeskim:mentions | umls-concept:C1418599 | lld:lifeskim |
pubmed-article:9158217 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:9158217 | pubmed:dateCreated | 1997-6-9 | lld:pubmed |
pubmed-article:9158217 | pubmed:abstractText | We describe a family with autosomal dominant polycystic kidney disease in which molecular typing with closely linked markers for the PKD1 and PKD2 genes indicated absence of linkage. Thus, a third still unknown locus appears likely to be involved in disease development. This is the fourth "PKD3-linked" family described to date and the first from Italy. | lld:pubmed |
pubmed-article:9158217 | pubmed:language | eng | lld:pubmed |
pubmed-article:9158217 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9158217 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:9158217 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:9158217 | pubmed:month | Nov | lld:pubmed |
pubmed-article:9158217 | pubmed:issn | 0272-6386 | lld:pubmed |
pubmed-article:9158217 | pubmed:author | pubmed-author:PignattiP FPF | lld:pubmed |
pubmed-article:9158217 | pubmed:author | pubmed-author:TenconiRR | lld:pubmed |
pubmed-article:9158217 | pubmed:author | pubmed-author:ClementiMM | lld:pubmed |
pubmed-article:9158217 | pubmed:author | pubmed-author:RossettiSS | lld:pubmed |
pubmed-article:9158217 | pubmed:author | pubmed-author:TurcoA EAE | lld:pubmed |
pubmed-article:9158217 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:9158217 | pubmed:volume | 28 | lld:pubmed |
pubmed-article:9158217 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:9158217 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:9158217 | pubmed:pagination | 759-61 | lld:pubmed |
pubmed-article:9158217 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:meshHeading | pubmed-meshheading:9158217-... | lld:pubmed |
pubmed-article:9158217 | pubmed:year | 1996 | lld:pubmed |
pubmed-article:9158217 | pubmed:articleTitle | An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene. | lld:pubmed |
pubmed-article:9158217 | pubmed:affiliation | Institute of Genetics, University of Verona School of Medicine, University Hospital Polyclinic Borgo Roma, Italy. | lld:pubmed |
pubmed-article:9158217 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:9158217 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9158217 | lld:pubmed |