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Integrating Tumor Sequencing Into Clinical Practice for Patients With Mismatch Repair-Deficient Lync...

Integrating Tumor Sequencing Into Clinical Practice for Patients With Mismatch Repair-Deficient Lync...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8373535

Integrating Tumor Sequencing Into Clinical Practice for Patients With Mismatch Repair-Deficient Lynch Syndrome Spectrum Cancers

About this item

Full title

Integrating Tumor Sequencing Into Clinical Practice for Patients With Mismatch Repair-Deficient Lynch Syndrome Spectrum Cancers

Publisher

United States: Wolters Kluwer

Journal title

Clinical and translational gastroenterology, 2021-08, Vol.12 (8), p.e00397-e00397

Language

English

Formats

Publication information

Publisher

United States: Wolters Kluwer

More information

Scope and Contents

Contents

Uninformative germline genetic testing presents a challenge to clinical management for patients suspected to have Lynch syndrome, a cancer predisposition syndrome caused by germline variants in the mismatch repair (MMR) genes or EPCAM.
Among a consecutive series of MMR-deficient Lynch syndrome spectrum cancers identified through immunohistochemi...

Alternative Titles

Full title

Integrating Tumor Sequencing Into Clinical Practice for Patients With Mismatch Repair-Deficient Lynch Syndrome Spectrum Cancers

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8373535

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8373535

Other Identifiers

ISSN

2155-384X

E-ISSN

2155-384X

DOI

10.14309/ctg.0000000000000397

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