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Article

p53 Germline mutation in a patient with Li-Fraumeni Syndrome and three metachronous malignancies

1 Aug 2002

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12200603
DOI: 10.1007/s00432-002-0360-3

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Related research

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p53 Germline mutation in a patient with Li-Fraumeni Syndrome and three metachronous malignanciesPMID 12200603Read ↗

Germline TP53 mutations and Li-Fraumeni syndrome.Semantic proximity Read ↗

Genetic analysis in a patient with nine primary malignant neoplasms: a rare case of Li-Fraumeni syndrome.Semantic proximity Read ↗

Genetic and functional studies of a germline TP53 splicing mutation in a Li–Fraumeni-like familySemantic proximity Read ↗

A child with Li-Fraumeni syndrome: Modes to inactivate the second allele of TP53 in three different malignancies.Semantic proximity Read ↗

Germline mutations of p53 tumor gene linked to Li-Fraumeni syndrome (LFS) are associated with an increased risk of cancerSemantic proximity Read ↗

[TP53 germline mutation related Li-Fraumeni syndrome: report of a case].Semantic proximity Read ↗

Detection of 11 germline inactivating TP53 mutations and absence of TP63 andHCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndromeSemantic proximity Read ↗

A patient with four metachronous cancers and multiple adenomatous colon polyps harboring the American Founder Lynch syndrome mutation: a case reportSemantic proximity Read ↗

Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutationSemantic proximity Read ↗

p53 and the Li-Fraumeni syndromeSemantic proximity Read ↗

A novel, de novo germline TP53 mutation in a rare presentation of the Li-Fraumeni syndrome in the maxilla.Semantic proximity Read ↗

Li-Fraumeni syndrome and the role of the p53 tumor suppressor gene in cancer susceptibility.Semantic proximity Read ↗

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