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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2004-9-2
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pubmed:abstractText |
The hallmark of Li-Fraumeni syndrome (LFS), a familial cancer syndrome, is constitutional TP53 mutation. The authors addressed the complex question of predictive prenatal genetic testing for cancer risk associated with inheritance of TP53 mutation.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1077-4114
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pubmed:author |
pubmed-author:AvigadSmadarS,
pubmed-author:BarelDalitD,
pubmed-author:Ben-BaruchNoaN,
pubmed-author:BenyaminyHadarH,
pubmed-author:CohenIan JIJ,
pubmed-author:GoshenYacovY,
pubmed-author:PelegDanD,
pubmed-author:ShohatMordechaiM,
pubmed-author:TaubEllenE,
pubmed-author:YanivIsaacI,
pubmed-author:ZaizovRinaR
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pubmed:issnType |
Print
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
541-5
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pubmed:dateRevised |
2011-10-6
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pubmed:meshHeading |
pubmed-meshheading:15342977-Adult,
pubmed-meshheading:15342977-Female,
pubmed-meshheading:15342977-Genes, p53,
pubmed-meshheading:15342977-Genetic Counseling,
pubmed-meshheading:15342977-Genetic Predisposition to Disease,
pubmed-meshheading:15342977-Germ-Line Mutation,
pubmed-meshheading:15342977-Heterozygote,
pubmed-meshheading:15342977-Humans,
pubmed-meshheading:15342977-Infant,
pubmed-meshheading:15342977-Li-Fraumeni Syndrome,
pubmed-meshheading:15342977-Male,
pubmed-meshheading:15342977-Pedigree,
pubmed-meshheading:15342977-Pregnancy,
pubmed-meshheading:15342977-Prenatal Diagnosis,
pubmed-meshheading:15342977-Rhabdomyosarcoma
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pubmed:year |
2004
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pubmed:articleTitle |
Prenatal diagnosis in Li-Fraumeni syndrome.
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pubmed:affiliation |
Molecular Oncology, Felsenstein Medical Research Center, Petah Tikva, Israel. savigad@post.tau.ac.il
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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