Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2006-3-2
pubmed:abstractText
The Muir-Torre syndrome is a rare autosomal dominant condition and is currently considered a subtype of the more common hereditary nonpolyposis colorectal cancer syndrome, in which multiple primary malignancies occur together with sebaceous gland tumors.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-10534628, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-10894967, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-11859205, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-12641777, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-12776718, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-14988697, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-15166510, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-15662714, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-15839358, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-5684233, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-6020987, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-7601953, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-7712655, http://linkedlifedata.com/resource/pubmed/commentcorrection/16466577-9732950
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:issn
1477-7819
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
4
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
8
pubmed:dateRevised
2009-11-18
pubmed:year
2006
pubmed:articleTitle
Sebaceous gland tumors and internal malignancy in the context of Muir-Torre syndrome. A case report and review of the literature.
pubmed:affiliation
Fourth Department of Surgery, Aristotle University of Thessaloniki, Greece. ctsalis@med.auth.gr
pubmed:publicationType
Journal Article