| pubmed-article:10876191 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10876191 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:10876191 | lifeskim:mentions | umls-concept:C0678226 | lld:lifeskim |
| pubmed-article:10876191 | lifeskim:mentions | umls-concept:C1833921 | lld:lifeskim |
| pubmed-article:10876191 | lifeskim:mentions | umls-concept:C0694890 | lld:lifeskim |
| pubmed-article:10876191 | lifeskim:mentions | umls-concept:C1861403 | lld:lifeskim |
| pubmed-article:10876191 | lifeskim:mentions | umls-concept:C0543431 | lld:lifeskim |
| pubmed-article:10876191 | lifeskim:mentions | umls-concept:C0003442 | lld:lifeskim |
| pubmed-article:10876191 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:10876191 | pubmed:dateCreated | 2000-8-1 | lld:pubmed |
| pubmed-article:10876191 | pubmed:abstractText | Multiple endocrine neoplasia type 2 (MEN 2) and familial medullary thyroid carcinoma (FMTC) are autosomal dominantly inherited cancer syndromes that predispose to C-cell hyperplasia and MTC. MEN 2A and FMTC are caused by mutations in the RET proto-oncogene. | lld:pubmed |
| pubmed-article:10876191 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10876191 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10876191 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:10876191 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:10876191 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10876191 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10876191 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10876191 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:10876191 | pubmed:issn | 0039-6060 | lld:pubmed |
| pubmed-article:10876191 | pubmed:author | pubmed-author:JacksonC ECE | lld:pubmed |
| pubmed-article:10876191 | pubmed:author | pubmed-author:FeldmanG LGL | lld:pubmed |
| pubmed-article:10876191 | pubmed:author | pubmed-author:SaxeA WAW | lld:pubmed |
| pubmed-article:10876191 | pubmed:author | pubmed-author:AinsworthP... | lld:pubmed |
| pubmed-article:10876191 | pubmed:author | pubmed-author:EdmondsM WMW | lld:pubmed |
| pubmed-article:10876191 | pubmed:author | pubmed-author:LenoirG MGM | lld:pubmed |
| pubmed-article:10876191 | pubmed:author | pubmed-author:Schuffenecker... | lld:pubmed |
| pubmed-article:10876191 | pubmed:author | pubmed-author:TalposG BGB | lld:pubmed |
| pubmed-article:10876191 | pubmed:author | pubmed-author:RobersonJJ | lld:pubmed |
| pubmed-article:10876191 | pubmed:author | pubmed-author:PetrucelliNN | lld:pubmed |
| pubmed-article:10876191 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10876191 | pubmed:volume | 128 | lld:pubmed |
| pubmed-article:10876191 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10876191 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10876191 | pubmed:pagination | 93-8 | lld:pubmed |
| pubmed-article:10876191 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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| pubmed-article:10876191 | pubmed:year | 2000 | lld:pubmed |
| pubmed-article:10876191 | pubmed:articleTitle | Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG-->ATG) mutation. | lld:pubmed |
| pubmed-article:10876191 | pubmed:affiliation | Department of Medical Genetics, Henry Ford Hospital, the Center for Molecular Medicine and Genetics, Detroit, MI 48201, USA. | lld:pubmed |
| pubmed-article:10876191 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10876191 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:10876191 | lld:pubmed |
