(Q37595344)

English

Disentangling the Babylonian speech confusion in genetic counseling: an analysis of the reliability and validity of the nomenclature for BRCA1/2 DNA-test results other than pathogenic

scientific article published on October 2009

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scholarly article

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Europe PubMed Central

PubMed publication ID

21 August 2017

1 reference

Europe PubMed Central

Disentangling the Babylonian speech confusion in genetic counseling: an analysis of the reliability and validity of the nomenclature for BRCA1/2 DNA-test results other than pathogenic (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

object named as

Aad Tibben

5

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Anne M Stiggelbout

object named as

Anne M Stiggelbout

4

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Christi J van Asperen

2

object named as

Christi J van Asperen

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

author name string

Joël Vos

1

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

Juul T Wijnen

3

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Europe PubMed Central

PubMed publication ID

21 August 2017

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publication date

1 October 2009

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Europe PubMed Central

PubMed publication ID

21 August 2017

Genetics in Medicine

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Europe PubMed Central

PubMed publication ID

21 August 2017

11

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Europe PubMed Central

PubMed publication ID

21 August 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

742-749

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

Guidelines for human gene nomenclature

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

Meta-analysis of BRCA1 and BRCA2 penetrance

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

The counsellees' view of an unclassified variant in BRCA1/2: recall, interpretation, and impact on life.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

No evidence of false reassurance among women with an inconclusive BRCA1/2 genetic test result

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

What's the message? Interpretation of an uninformative BRCA1/2 test result for women at risk of familial breast cancer

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

Clinician perspectives about molecular genetic testing for heritable conditions and development of a clinician-friendly laboratory report

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

Genetic Testing for Women Previously Diagnosed with Breast/Ovarian Cancer: Examining the Impact of BRCA1 and BRCA2 Mutation Searching

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B2E608

21 January 2018

Identifiers

10.1097/GIM.0B013E3181B2E608

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

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