Log in to save to my catalogue

Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition...

Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2871490000

Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients

About this item

Full title

Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients

Publisher

England: Nature Publishing Group

Journal title

European journal of human genetics : EJHG, 2023-10, Vol.31 (10), p.1139-1146

Language

English

Formats

Publication information

Publisher

England: Nature Publishing Group

More information

Scope and Contents

Contents

The prevalence of pathogenic and likely pathogenic (P/LP) variants in genes associated with cancer predisposition syndromes (CPS) is estimated to be 8-18% for paediatric cancer patients. In more than half of the carriers, the family history is unsuspicious for CPS. Therefore, broad genetic testing could identify germline predisposition in additiona...

Alternative Titles

Full title

Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2871490000

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2871490000

Other Identifiers

ISSN

1018-4813

E-ISSN

1476-5438

DOI

10.1038/s41431-023-01423-8

How to access this item