pubmed-article:12011148 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12011148 | lifeskim:mentions | umls-concept:C1333990 | lld:lifeskim |
pubmed-article:12011148 | lifeskim:mentions | umls-concept:C0008633 | lld:lifeskim |
pubmed-article:12011148 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:12011148 | lifeskim:mentions | umls-concept:C0879389 | lld:lifeskim |
pubmed-article:12011148 | lifeskim:mentions | umls-concept:C0018591 | lld:lifeskim |
pubmed-article:12011148 | lifeskim:mentions | umls-concept:C0206243 | lld:lifeskim |
pubmed-article:12011148 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:12011148 | pubmed:dateCreated | 2002-5-15 | lld:pubmed |
pubmed-article:12011148 | pubmed:abstractText | The mismatch repair gene, MLH1, appears to occur as two main haplotypes at least in white populations. These are referred to as A and G types with reference to the A/G polymorphism at IVS14-19. On the basis of preliminary experimental data, we hypothesised that deviations from the expected frequency of these two haplotypes could exist in carriers of disease associated MLH1 germline mutations. | lld:pubmed |
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pubmed-article:12011148 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12011148 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12011148 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12011148 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:12011148 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12011148 | pubmed:language | eng | lld:pubmed |
pubmed-article:12011148 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12011148 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:12011148 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12011148 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12011148 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12011148 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12011148 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12011148 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12011148 | pubmed:month | May | lld:pubmed |
pubmed-article:12011148 | pubmed:issn | 1468-6244 | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:WuJJ | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:BurgMM | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:ChongGG | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:FarberDD | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:ThibodeauS... | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:WijnenJJ | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:HamelNN | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:MacNamaraEE | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:BapatBB | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:FoulkesW DWD | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:HutterPP | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:HeinimannKK | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:Rey-BerthodCC | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:ThiffaultII | lld:pubmed |
pubmed-article:12011148 | pubmed:author | pubmed-author:VerkuijlenPP | lld:pubmed |
pubmed-article:12011148 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:12011148 | pubmed:volume | 39 | lld:pubmed |
pubmed-article:12011148 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12011148 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12011148 | pubmed:pagination | 323-7 | lld:pubmed |
pubmed-article:12011148 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
pubmed-article:12011148 | pubmed:meshHeading | pubmed-meshheading:12011148... | lld:pubmed |
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pubmed-article:12011148 | pubmed:year | 2002 | lld:pubmed |
pubmed-article:12011148 | pubmed:articleTitle | An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1. | lld:pubmed |
pubmed-article:12011148 | pubmed:affiliation | Unit of Genetics, Institut Central des Hôpitaux Valaisans, Sion, Switzerland. pierre.hutter@ichv.vsnet.ch | lld:pubmed |
pubmed-article:12011148 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:12011148 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:12011148 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:12011148 | lld:pubmed |