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Article

A tailored approach to BRAF and MLH1 methylation testing in a universal screening program for Lynch syndrome

6 Jan 2017

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 28059100
DOI: 10.1038/modpathol.2016.211

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Related research

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A tailored approach to BRAF and MLH1 methylation testing in a universal screening program for Lynch syndromePMID 28059100Read ↗

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Risk assessment and genetic counseling for Lynch syndrome – Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal CancerSemantic proximity Read ↗

Canadian consensus for the assessment and testing of Lynch syndromeSemantic proximity Read ↗

Evaluating the impact of universal Lynch syndrome screening in a publicly funded healthcare system.Semantic proximity Read ↗

Genetic Counseling and Surveillance Focused on Lynch SyndromeSemantic proximity Read ↗

Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch SyndromeSemantic proximity Read ↗

Impact of an immunohistochemistry-based universal screening protocol for Lynch syndrome in endometrial cancer on genetic counseling and testingSemantic proximity Read ↗

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome.Semantic proximity Read ↗

Lessons learnt from implementation of a Lynch syndrome screening program for patients with gynaecological malignancy.Semantic proximity Read ↗

Lynch syndrome among gynecologic oncology patients meeting Bethesda guidelines for screeningSemantic proximity Read ↗

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