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pubmed-article:18349092pubmed:abstractTextIndividuals with Li-Fraumeni syndrome (LFS) have an inherited cancer predisposition to a diverse array of malignancies beginning early in life; survivors of one cancer have a markedly elevated risk of additional primary tumors. The underlying genetic defect in the majority of the families is a germline mutation in the TP53 tumor suppressor gene. The diversity of tumors and rarity of families have contributed to the difficulty in devising effective screening recommendations for members of LFS kindreds.lld:pubmed
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pubmed-article:18349092pubmed:articleTitleF18-fluorodeoxyglucose-positron emission tomography/computed tomography screening in Li-Fraumeni syndrome.lld:pubmed
pubmed-article:18349092pubmed:affiliationDivision of Population Sciences, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA.lld:pubmed
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