(Q35443388)

English

Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancer

scientific article

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scholarly article

1 reference

Europe PubMed Central

8 August 2017

Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancer (English)

1 reference

Europe PubMed Central

8 August 2017

colorectal cancer

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

colorectal carcinoma

1 reference

based on heuristic

inferred from title

Steven A. Narod

2

object named as

S A Narod

1 reference

Europe PubMed Central

8 August 2017

author name string

P Watson

1

1 reference

Europe PubMed Central

8 August 2017

R Fodde

3

1 reference

Europe PubMed Central

8 August 2017

A Wagner

4

1 reference

Europe PubMed Central

8 August 2017

J F Lynch

5

1 reference

Europe PubMed Central

8 August 2017

S T Tinley

6

1 reference

Europe PubMed Central

8 August 2017

C L Snyder

7

1 reference

Europe PubMed Central

8 August 2017

S A Coronel

8

1 reference

Europe PubMed Central

8 August 2017

B Riley

9

1 reference

Europe PubMed Central

8 August 2017

Y Kinarsky

10

1 reference

Europe PubMed Central

8 August 2017

H T Lynch

11

1 reference

Europe PubMed Central

8 August 2017

language of work or name

0 references

publication date

1 August 2003

1 reference

Europe PubMed Central

8 August 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

8 August 2017

40

1 reference

Europe PubMed Central

8 August 2017

8

1 reference

Europe PubMed Central

8 August 2017

591-596

1 reference

Europe PubMed Central

8 August 2017

Hereditary breast-ovarian cancer at the bedside: role of the medical oncologist

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

27 July 2018

Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

27 July 2018

Psychological consequences of predictive genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a prospective follow-up study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

27 July 2018

Genetic susceptibility to non-polyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

27 July 2018

Recommendations for follow-up care of individuals with an inherited predisposition to cancer. I. Hereditary nonpolyposis colon cancer. Cancer Genetics Studies Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

27 July 2018

Consent, confidentiality, and research.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

27 July 2018

Family information service and hereditary cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

26 September 2018

Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer. Part II: Hereditary nonpolyposis colorectal carcinoma as a model.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

26 September 2018

Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer. Part I: Studies of cancer in families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

26 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

26 September 2018

Patients' attitudes about autonomy and confidentiality in genetic testing for breast-ovarian cancer susceptibility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

26 September 2018

BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735553

26 September 2018

Disclosure to the family of breast/ovarian cancer genetic test results: patient's willingness and associated factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/12920070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prophylactic mastectomy: obstacles and benefits

1 reference

https://pubmed.ncbi.nlm.nih.gov/12920070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficacy of bilateral prophylactic mastectomy in BRCA1 and BRCA2 gene mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/12920070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Voluntary disclosure of BRCA1 mutation test results

1 reference

https://pubmed.ncbi.nlm.nih.gov/12920070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is there a role for prophylactic subtotal colectomy among hereditary nonpolyposis colorectal cancer germline mutation carriers?

1 reference

https://pubmed.ncbi.nlm.nih.gov/12920070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.40.8.591

1 reference

Europe PubMed Central

8 August 2017

1 reference

Europe PubMed Central

8 August 2017

1 reference

Europe PubMed Central

8 August 2017

ResearchGate publication ID

0 references

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