(Q36087551)

12 August 2017

Mutation deep within an intron of MSH2 causes Lynch syndrome (English)

1 reference

12 August 2017

Bryony Thompson

6

0 references

Christophe Rosty

Christophe Rosty

5

0 references

Daniel D Buchanan

Daniel D Buchanan

2

0 references

Mark Jenkins

Mark A Jenkins

9

0 references

Amanda Spurdle

Amanda B Spurdle

7

0 references

John Hopper

8

John L Hopper

1 reference

12 August 2017

Mark Clendenning

1

1 reference

12 August 2017

Michael D Walsh

3

1 reference

12 August 2017

Belinda Nagler

4

1 reference

12 August 2017

Joanne P Young

10

1 reference

12 August 2017

1 June 2011

1 reference

12 August 2017

1 reference

12 August 2017

10

1 reference

12 August 2017

2

1 reference

12 August 2017

297-301

1 reference

12 August 2017

Cancer statistics, 2010

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4580736

Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4580736

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4580736

Clonal transformation of adult human leukocytes by Epstein-Barr virus

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4580736

Mismatch repair gene polymorphisms and survival in invasive ovarian cancer patients

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4580736

A novel donor splice site in intron 11 of the CFTR gene, created by mutation 1811+1.6kbA-->G, produces a new exon: high frequency in Spanish cystic fibrosis chromosomes and association with severe phenotype.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4580736

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

11 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-011-9427-0

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-011-9427-0

Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-011-9427-0

Origins and prevalence of the American Founder Mutation of MSH2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-011-9427-0

Genetic investigation of DNA-repair pathway genesPMS2,MLH1,MSH2,MSH6,MUTYH,OGG1 andMTH1 in sporadic colon cancer

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21360204

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21360204

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10689-011-9427-0

1 reference

12 August 2017

1 reference

12 August 2017

PubMed publication ID

21360204

1 reference