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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2010-5-14
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pubmed:abstractText |
Cowden syndrome (CS) is a rare autosomal dominant disorder with an increased risk of breast, thyroid and uterine cancer development. The International Cowden Consortium has defined strict diagnostic criteria for individuals and families suspected of having CS.
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pubmed:language |
slo
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
0862-495X
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
23
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
111-4
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pubmed:meshHeading |
pubmed-meshheading:20465090-Adult,
pubmed-meshheading:20465090-Female,
pubmed-meshheading:20465090-Germ-Line Mutation,
pubmed-meshheading:20465090-Hamartoma Syndrome, Multiple,
pubmed-meshheading:20465090-Humans,
pubmed-meshheading:20465090-Male,
pubmed-meshheading:20465090-Middle Aged,
pubmed-meshheading:20465090-Nucleic Acid Amplification Techniques,
pubmed-meshheading:20465090-PTEN Phosphohydrolase,
pubmed-meshheading:20465090-Sequence Analysis, DNA
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pubmed:year |
2010
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pubmed:articleTitle |
[Our experience with analysis of the PTEN gene in patients suspected of having Cowden syndrome].
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pubmed:affiliation |
Ostav biologie a lékarské genetiky, FN Motol a 2. LF UK, V Uvalu 84, 150 06 Praha 5. pevas78@centrum.cz
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pubmed:publicationType |
Journal Article,
English Abstract
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