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Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotyp...

Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotyp...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b0d0d2ac94f64fffbf87379d9c7606cb

Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation

About this item

Full title

Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation

Publisher

England: BioMed Central Ltd

Journal title

BMC medical genomics, 2022-03, Vol.15 (1), p.44-44, Article 44

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Li-Fraumeni syndrome (LFS) is a rare autosomal hereditary predisposition to multiples cancers, mainly affecting young individuals. It is characterized by a broad tumor spectrum. To our best knowledge, only one Tunisian study with a confirmed LFS was published.
Our study focused on the clinical, histopathological and genetic results of two patien...

Alternative Titles

Full title

Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_b0d0d2ac94f64fffbf87379d9c7606cb

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b0d0d2ac94f64fffbf87379d9c7606cb

Other Identifiers

ISSN

1755-8794

E-ISSN

1755-8794

DOI

10.1186/s12920-022-01189-w

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