(Q47301537)

13 January 2018

title

Hereditary nonpolyposis colorectal carcinoma (HNPCC) and HNPCC-like families: Problems in diagnosis, surveillance, and management (English)

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13 January 2018

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Henry T Lynch

1

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13 January 2018

Bronson D Riley

2

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13 January 2018

Scott M Weissman

3

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13 January 2018

Stephanie M Coronel

4

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13 January 2018

Yulia Kinarsky

5

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13 January 2018

Jane F Lynch

6

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13 January 2018

Trudy G Shaw

7

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13 January 2018

Wendy S Rubinstein

8

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13 January 2018

language of work or name

English

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publication date

1 January 2004

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13 January 2018

published in

Cancer

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13 January 2018

volume

100

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13 January 2018

issue

1

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13 January 2018

page(s)

53-64

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13 January 2018

Hereditary non-polyposis colorectal cancer — morphologies, genes and mutations

cites work

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

Hereditary colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Muir-Torre syndrome in several members of a family with a variant of the Cancer Family Syndrome

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Role of DNA mismatch repair defects in the pathogenesis of human cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Failure to diagnose hereditary colorectal cancer and its medicolegal implications: a hereditary nonpolyposis colorectal cancer case

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

A descriptive study of BRCA1 testing and reactions to disclosure of test results

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

An update on DNA-based BRCA1/BRCA2 genetic counseling in hereditary breast cancer.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

A 10-Mb paracentric inversion of chromosome arm 2p inactivatesMSH2 and is responsible for hereditary nonpolyposis colorectal cancer in a North-American kindred

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Familial endometrial cancer in female carriers of MSH6 germline mutations

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Family information service and hereditary cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Laws restricting health insurers' use of genetic information: impact on genetic discrimination

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Life insurance and breast cancer risk assessment: Adverse selection, genetic testing decisions, and discrimination

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Patients' fear of genetic discrimination by health insurers: the impact of legal protections.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Developing culturally sensitive cancer genetics communication aids for African Americans

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Commercialization of BRCA1/2 testing: practitioner awareness and use of a new genetic test

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

The use and interpretation of commercial APC gene testing for familial adenomatous polyposis

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Hereditary proximal colonic cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Evolution of hereditary non-polyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Attenuated familial adenomatous polyposis (AFAP). A phenotypically and genotypically distinctive variant of FAP.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Cumulative incidence of colorectal and extracolonic cancers in MLH1 and MSH2 mutation carriers of hereditary nonpolyposis colorectal cancer.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

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

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the Philadelphia chromosome

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11912

7 January 2021

Identifiers

DOI

10.1002/CNCR.11912

1 reference

13 January 2018

1 reference

13 January 2018