Characterization of a novel founderMSH6mutation causing Lynch syndrome in the French Canadian population

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Germline MSH6 Mutation in a Patient With Two Independent Primary Glioblastomas.Recent progress in Lynch syndrome and other familial colorectal cancer syndromes.

P2860

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Characterization of a novel founderMSH6mutation causing Lynch syndrome in the French Canadian population

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http://www.wikidata.org/entity/Q58325135

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article

@en

im November 2014 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в листопаді 2014

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Characterization of a novel fo ...... the French Canadian population

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Characterization of a novel fo ...... the French Canadian population

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Item

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Characterization of a novel fo ...... the French Canadian population

@en

Characterization of a novel fo ...... the French Canadian population

@nl

prefLabel

Characterization of a novel fo ...... the French Canadian population

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Characterization of a novel fo ...... the French Canadian population

@nl

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Characterization of a novel fo ...... the French Canadian population

@en

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A Gologan

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A Roussel-Jobin

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A Volenik

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B Maranda

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D Provencher

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F Rousseau

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G Chong

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J Latreille

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J Liu

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K Australie

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P2860

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome

Familial endometrial cancer in female carriers of MSH6 germline mutations

Risks of Lynch syndrome cancers for MSH6 mutation carriers.

Cancer risk in MLH1, MSH2 and MSH6 mutation carriers; different risk profiles may influence clinical management.

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

High-resolution multipoint linkage-disequilibrium mapping in the context of a human genome sequence.

A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting.

A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome.

No MSH6 germline mutations in breast cancer families with colorectal and/or endometrial cancer

Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome

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536-542

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scholarly article

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10.1111/CGE.12526

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http://www.w3.org/2001/XMLSchema#string

P478

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Anne-Marie Mes-Masson

William D Foulkes

Celia Greenwood

Ester Castellsagué

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2014-11-22T00:00:00Z

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25318681

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Characterization of a novel founderMSH6mutation causing Lynch syndrome in the French Canadian population

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P2860

P2860

Characterization of a novel founderMSH6mutation causing Lynch syndrome in the French Canadian population

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698