(Q58325135)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25318681%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

title

Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population (English)

1 reference

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21 February 2020

1 reference

1

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21 February 2020

Celia Greenwood

20

1 reference

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21 February 2020

Anne-Marie Mes-Masson

21

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21 February 2020

William David Foulkes

26

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21 February 2020

author name string

J Liu

2

1 reference

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21 February 2020

A Volenik

3

1 reference

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21 February 2020

S Giroux

4

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21 February 2020

R Gagné

5

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21 February 2020

B Maranda

6

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21 February 2020

A Roussel-Jobin

7

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21 February 2020

J Latreille

8

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21 February 2020

R Laframboise

9

1 reference

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21 February 2020

L Palma

10

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21 February 2020

L Kasprzak

11

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21 February 2020

V A Marcus

12

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21 February 2020

M Breguet

13

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21 February 2020

S Nolet

14

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21 February 2020

Z El-Haffaf

15

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21 February 2020

K Australie

16

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21 February 2020

A Gologan

17

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21 February 2020

O Aleynikova

18

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21 February 2020

K Oros-Klein

19

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21 February 2020

D Provencher

22

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21 February 2020

M Tischkowitz

23

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21 February 2020

G Chong

24

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21 February 2020

F Rousseau

25

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21 February 2020

publication date

22 November 2014

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21 February 2020

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21 February 2020

volume

87

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21 February 2020

issue

6

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21 February 2020

page(s)

536-542

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Detection of genetic alterations in hereditary colorectal cancer screening

21 February 2020

cites work

1 reference

Risk of breast cancer in Lynch syndrome: a systematic review.

21 January 2018

1 reference

Inherited susceptibility to common cancers

21 January 2018

1 reference

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

21 January 2018

1 reference

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance

21 January 2018

1 reference

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

21 January 2018

1 reference

Risks of Lynch syndrome cancers for MSH6 mutation carriers

21 January 2018

1 reference

Familial endometrial cancer in female carriers of MSH6 germline mutations

21 January 2018

1 reference

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

21 January 2018

1 reference

Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome.

21 January 2018

1 reference

Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

DMLE+: Bayesian linkage disequilibrium gene mapping.

21 January 2018

1 reference

Constitutional mismatch repair-deficiency syndrome

21 January 2018

1 reference

Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/CGE.12526

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25318681%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

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