Log in to save to my catalogue

Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and...

Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e22f263cf37d4328b380d9088edc9000

Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity

About this item

Full title

Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity

Publisher

England: BioMed Central Ltd

Journal title

Breast cancer research : BCR, 2018-08, Vol.20 (1), p.87-87, Article 87

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Breast cancer is the most prevalent tumor entity in Li-Fraumeni syndrome. Up to 80% of individuals with a Li-Fraumeni-like phenotype do not harbor detectable causative germline TP53 variants. Yet, no systematic panel analyses for a wide range of cancer predisposition genes have been conducted on cohorts of women with breast cancer fulfilling Li-Fra...

Alternative Titles

Full title

Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_e22f263cf37d4328b380d9088edc9000

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e22f263cf37d4328b380d9088edc9000

Other Identifiers

ISSN

1465-542X,1465-5411

E-ISSN

1465-542X

DOI

10.1186/s13058-018-1011-1

How to access this item