PREMM5 distinguishes sporadic from Lynch syndrome-associated MMR-deficient/MSI-high colorectal cancer
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Title
PREMM5 distinguishes sporadic from Lynch syndrome-associated MMR-deficient/MSI-high colorectal cancer
Authors
Keywords
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Journal
Familial Cancer
Volume 22, Issue 4, Pages 459-465
Publisher
Springer Science and Business Media LLC
Online
2023-08-12
DOI
10.1007/s10689-023-00345-0
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- Current Genetic Service Delivery Models for the Provision of Genetic Testing in Europe: A Systematic Review of the Literature
- (2019) Brigid Unim et al. Frontiers in Genetics
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- (2019) Adriana Della Valle et al. EUROPEAN JOURNAL OF CANCER
- Use of Family History and Genetic Testing to Determine Risk of Colorectal Cancer
- (2019) Fay Kastrinos et al. GASTROENTEROLOGY
- Guidelines for the management of hereditary colorectal cancer from the British Society of Gastroenterology (BSG)/Association of Coloproctology of Great Britain and Ireland (ACPGBI)/United Kingdom Cancer Genetics Group (UKCGG)
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- Development and Validation of the PREMM5 Model for Comprehensive Risk Assessment of Lynch Syndrome
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- Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer
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- (2016) Marcia Cruz-Correa et al. Journal of Genetic Counseling
- Population-Based Lynch Syndrome Screening by Microsatellite Instability in Patients ≤50: Prevalence, Testing Determinants and Result Availability Prior to Colon Surgery
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