(Q44511151)

3 December 2017

title

The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome (English)

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3 December 2017

Susan Stuckless

1

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3 December 2017

Patrick S Parfrey

2

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3 December 2017

Michael O Woods

3

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3 December 2017

Janet Cox

4

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3 December 2017

G William Fitzgerald

5

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3 December 2017

Jane S Green

6

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3 December 2017

Roger C Green

7

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3 December 2017

publication date

1 January 2007

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3 December 2017

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3 December 2017

volume

6

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3 December 2017

issue

1

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3 December 2017

page(s)

1-12

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https://scigraph.springernature.com/pub.10.1007/s10689-006-0014-8

3 December 2017

exact match

0 references

cites work

Clinical phenotype and prevalence of hereditary nonpolyposis colorectal cancer syndrome in Chinese population

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10689-006-0014-8

The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer

21 January 2018

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12 December 2020

A frequent hMSH2 mutation in hereditary non-polyposis colon cancer syndrome

1 reference

12 December 2020

The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas

1 reference

12 December 2020

DNA mismatch repair genes and colorectal cancer

1 reference

12 December 2020

Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis

1 reference

12 December 2020

Detection of mutations in mismatch repair genes in Portuguese families with hereditary non-polyposis colorectal cancer (HNPCC) by a multi-method approach

1 reference

12 December 2020

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

1 reference

12 December 2020

Frequency of hereditary non-polyposis colorectal cancer among Uruguayan patients with colorectal cancer

1 reference

12 December 2020

Impact of gender and parent of origin on the phenotypic expression of hereditary nonpolyposis colorectal cancer in a large Newfoundland kindred with a common MSH2 mutation

1 reference

12 December 2020

An update of HNPCC (Lynch syndrome).

1 reference

12 December 2020

Predominant germ-line mutation of the hMSH2 gene in Japanese hereditary non-polyposis colorectal cancer kindreds.

1 reference

12 December 2020

Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.

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12 December 2020

Recurrent germline mutation in MSH2 arises frequently de novo

1 reference

12 December 2020

Characterization of hereditary nonpolyposis colorectal cancer families from a population-based series of cases

1 reference

12 December 2020

Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations

1 reference

12 December 2020

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

1 reference

12 December 2020

Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and hMSH2 gene: correction for ascertainment

1 reference

12 December 2020

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

12 December 2020

Frequency of hereditary non-polyposis colorectal cancer and other colorectal cancer familial forms in Spain: a multicentre, prospective, nationwide study

1 reference

12 December 2020

Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer

1 reference

12 December 2020

Clinical and genetic epidemiology of inherited renal disease in Newfoundland

1 reference

12 December 2020

Genetic testing in hereditary colorectal cancer: indications and procedures

1 reference

12 December 2020

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

1 reference

12 December 2020

Population-based molecular detection of hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)

1 reference

12 December 2020

Frequent microsatellite instability and mismatch repair gene mutations in young Chinese patients with colorectal cancer

1 reference

12 December 2020

Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer

1 reference

12 December 2020

A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer

1 reference

12 December 2020

Hereditary colorectal cancer

1 reference

12 December 2020

Cancer risk in mismatch repair gene mutation carriers

1 reference

12 December 2020

Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer

1 reference

12 December 2020

Clinical definition of hereditary non-polyposis colorectal cancer: a search for the impossible?

1 reference

12 December 2020

Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients

1 reference

12 December 2020

Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1.

1 reference

12 December 2020

Tumor spectrum in cancer family syndrome (hereditary nonpolyposis colorectal cancer)

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12 December 2020

Germline truncating mutations in both MSH2 and BRCA2 in a single kindred

1 reference

12 December 2020

Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome.

1 reference

12 December 2020

Genetic mapping of a locus predisposing to human colorectal cancer

1 reference

12 December 2020

Germ line mutations of hMSH2 and hMLH1 genes in Japanese families with hereditary nonpolyposis colorectal cancer (HNPCC): usefulness of DNA analysis for screening and diagnosis of HNPCC patients

1 reference

12 December 2020

Inherited susceptibility to colorectal cancer

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12 December 2020

Frequency of hereditary non-polyposis colorectal cancer in Danish colorectal cancer patients

1 reference

12 December 2020

Extracolonic cancer in hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes

1 reference

12 December 2020

Family history of colorectal cancer in a Sweden county

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12 December 2020

Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes

1 reference

12 December 2020

High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes.

1 reference

12 December 2020

Cancer risk associated with germline DNA mismatch repair gene mutations

1 reference

12 December 2020

Cancer risk in mutation carriers of DNA-mismatch-repair genes

1 reference

12 December 2020

Hereditary non-polyposis colorectal cancer: current risks of colorectal cancer largely overestimated.

1 reference

12 December 2020

Recognition and treatment of patients with hereditary nonpolyposis colon cancer (Lynch syndromes I and II)

1 reference

12 December 2020

The incidence of Lynch syndrome

1 reference

12 December 2020

hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds

1 reference

12 December 2020

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

1 reference

12 December 2020

A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States

1 reference

12 December 2020

10.1007/S10689-006-0014-8

Identifiers

DOI

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3 December 2017

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