pubmed-article:2705471 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2705471 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:2705471 | lifeskim:mentions | umls-concept:C0199236 | lld:lifeskim |
pubmed-article:2705471 | lifeskim:mentions | umls-concept:C0010346 | lld:lifeskim |
pubmed-article:2705471 | lifeskim:mentions | umls-concept:C0080103 | lld:lifeskim |
pubmed-article:2705471 | lifeskim:mentions | umls-concept:C0017398 | lld:lifeskim |
pubmed-article:2705471 | lifeskim:mentions | umls-concept:C0439855 | lld:lifeskim |
pubmed-article:2705471 | lifeskim:mentions | umls-concept:C0080141 | lld:lifeskim |
pubmed-article:2705471 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
pubmed-article:2705471 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:2705471 | pubmed:dateCreated | 1989-5-19 | lld:pubmed |
pubmed-article:2705471 | pubmed:abstractText | We have analysed the pedigrees of 265 probands with Crohn disease, collected from a specialty clinic at the University of Düsseldorf. Complex segregation analysis suggests the presence of a recessive gene with incomplete penetrance for susceptibility to the disease with no residual causes of family resemblance. However, a proportion of the isolated cases are probably due to phenocopies, this proportion being greatest among cases with an advanced age of onset. | lld:pubmed |
pubmed-article:2705471 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2705471 | pubmed:language | eng | lld:pubmed |
pubmed-article:2705471 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2705471 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:2705471 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2705471 | pubmed:month | Jan | lld:pubmed |
pubmed-article:2705471 | pubmed:issn | 0148-7299 | lld:pubmed |
pubmed-article:2705471 | pubmed:author | pubmed-author:MajewskiFF | lld:pubmed |
pubmed-article:2705471 | pubmed:author | pubmed-author:KüsterWW | lld:pubmed |
pubmed-article:2705471 | pubmed:author | pubmed-author:FungWW | lld:pubmed |
pubmed-article:2705471 | pubmed:author | pubmed-author:PurrmannJJ | lld:pubmed |
pubmed-article:2705471 | pubmed:author | pubmed-author:PascoeLL | lld:pubmed |
pubmed-article:2705471 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2705471 | pubmed:volume | 32 | lld:pubmed |
pubmed-article:2705471 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2705471 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:2705471 | pubmed:pagination | 105-8 | lld:pubmed |
pubmed-article:2705471 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
pubmed-article:2705471 | pubmed:meshHeading | pubmed-meshheading:2705471-... | lld:pubmed |
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pubmed-article:2705471 | pubmed:meshHeading | pubmed-meshheading:2705471-... | lld:pubmed |
pubmed-article:2705471 | pubmed:year | 1989 | lld:pubmed |
pubmed-article:2705471 | pubmed:articleTitle | The genetics of Crohn disease: complex segregation analysis of a family study with 265 patients with Crohn disease and 5,387 relatives. | lld:pubmed |
pubmed-article:2705471 | pubmed:affiliation | Department of Dermatology, University of Düsseldorf, Federal Republic of Germany. | lld:pubmed |
pubmed-article:2705471 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:2705471 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:2705471 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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