| pubmed-article:3783618 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:3783618 | lifeskim:mentions | umls-concept:C0010674 | lld:lifeskim |
| pubmed-article:3783618 | lifeskim:mentions | umls-concept:C0026339 | lld:lifeskim |
| pubmed-article:3783618 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:3783618 | lifeskim:mentions | umls-concept:C0008661 | lld:lifeskim |
| pubmed-article:3783618 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:3783618 | lifeskim:mentions | umls-concept:C2828389 | lld:lifeskim |
| pubmed-article:3783618 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:3783618 | pubmed:dateCreated | 1986-12-31 | lld:pubmed |
| pubmed-article:3783618 | pubmed:abstractText | We have used multilocus analysis to exclude the cystic fibrosis locus from six polymorphic DNA markers covering most of chromosome 19. A substantial increase in the confidence for exclusion was obtained using the computer programme LINKAGE compared to analysis of pairwise lod scores. A structured approach to the analysis of linkage to autosomal recessive inherited diseases where the biochemical defect is not known is described. | lld:pubmed |
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| pubmed-article:3783618 | pubmed:language | eng | lld:pubmed |
| pubmed-article:3783618 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:3783618 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:3783618 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:3783618 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:3783618 | pubmed:issn | 0022-2593 | lld:pubmed |
| pubmed-article:3783618 | pubmed:author | pubmed-author:WilliamsonRR | lld:pubmed |
| pubmed-article:3783618 | pubmed:author | pubmed-author:WatsonEE | lld:pubmed |
| pubmed-article:3783618 | pubmed:author | pubmed-author:FarrallMM | lld:pubmed |
| pubmed-article:3783618 | pubmed:author | pubmed-author:WainwrightBB | lld:pubmed |
| pubmed-article:3783618 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:3783618 | pubmed:volume | 23 | lld:pubmed |
| pubmed-article:3783618 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:3783618 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:3783618 | pubmed:pagination | 417-20 | lld:pubmed |
| pubmed-article:3783618 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:3783618 | pubmed:year | 1986 | lld:pubmed |
| pubmed-article:3783618 | pubmed:articleTitle | A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19. | lld:pubmed |
| pubmed-article:3783618 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:3783618 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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