(Q43109049)

14 November 2017

BRCA2 mutations in hereditary breast and ovarian cancer in France (English)

1 reference

14 November 2017

1 reference

Dominique Stoppa-Lyonnet

3

object named as

Stoppa-Lyonnet D

1 reference

14 November 2017

Serova-Sinilnikova OM

1

1 reference

14 November 2017

Boutrand L

2

1 reference

14 November 2017

Bressac-de-Paillerets B

4

1 reference

14 November 2017

Dubois V

5

1 reference

14 November 2017

Lasset C

6

1 reference

14 November 2017

Janin N

7

1 reference

14 November 2017

Bignon YJ

8

1 reference

14 November 2017

Longy M

9

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14 November 2017

Maugard C

10

1 reference

14 November 2017

Lidereau R

11

1 reference

14 November 2017

Leroux D

12

1 reference

14 November 2017

Frebourg T

13

1 reference

14 November 2017

Mazoyer S

14

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14 November 2017

Lenoir GM

15

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14 November 2017

language of work or name

English

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publication date

1 May 1997

1 reference

American Journal of Human Genetics

14 November 2017

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14 November 2017

60

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14 November 2017

5

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14 November 2017

1236-1239

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Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes?

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

Mutation analysis of BRCA1 and BRCA2 in a male breast cancer population.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

Identification of the breast cancer susceptibility gene BRCA2

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation

1 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712433

Detecting single base substitutions as heteroduplex polymorphisms

1 December 2018

1 reference

12 December 2020

Rapid detection of single base mismatches as heteroduplexes on Hydrolink gels

1 reference

12 December 2020

Rapid detection of BRCA1 mutations by the protein truncation test

1 reference

12 December 2020

BRCA2 germline mutations in male breast cancer cases and breast cancer families

1 reference

12 December 2020

Mutations of the BRCA2 gene in ovarian carcinomas

1 reference

12 December 2020

A common mutation in BRCA2 that predisposes to a variety of cancers is found in both Jewish Ashkenazi and non-Jewish individuals

1 reference

12 December 2020

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

1 reference

12 December 2020

Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene

1 reference

12 December 2020

Identifiers

1 reference

14 November 2017

1 reference