(Q24813671)

5 July 2017

Strong evidence that the common variant S384F in BRCA2 has no pathogenic relevance in hereditary breast cancer (English)

1 reference

5 July 2017

9

Schmutzler RK

1 reference

5 July 2017

7

Arnold N

1 reference

5 July 2017

Barbara Wappenschmidt

1

object named as

Wappenschmidt B

1 reference

5 July 2017

6

Meindl A

1 reference

5 July 2017

Fimmers R

2

1 reference

5 July 2017

Rhiem K

3

1 reference

5 July 2017

Brosig M

4

1 reference

5 July 2017

Wardelmann E

5

1 reference

5 July 2017

Mallmann P

8

1 reference

5 July 2017

language of work or name

English

0 references

publication date

27 July 2005

1 reference

5 July 2017

Breast Cancer Research

1 reference

5 July 2017

7

1 reference

5 July 2017

R775-9

1 reference

5 July 2017

5

1 reference

Strategies for multilocus linkage analysis in humans

5 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1242149

RAD51 interacts with the evolutionarily conserved BRC motifs in the human breast cancer susceptibility gene brca2

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1242149

Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1242149

A full-likelihood method for the evaluation of causality of sequence variants from family data

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1242149

Limited relevance of the CHEK2 gene in hereditary breast cancer.

28 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FBCR1291

Loss of heterozygosity analysis at theBRCAloci in tumor samples from patients with familial breast cancer

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FBCR1291

Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16168123

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16168123

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Association of allelic losses on human chromosomal arms 11q and 16q in sporadic breast cancer

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16168123

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/BCR1291

1 reference

Dimensions Publication ID

5 July 2017

0 references

1 reference

5 July 2017

1 reference