(Q33289529)

25 July 2017

Multiplex SNaPshot for detection of BRCA1/2 common mutations in Spanish and Spanish related breast/ovarian cancer families (English)

1 reference

25 July 2017

1 reference

6

Angel Carracedo

1 reference

25 July 2017

Sandra Filippini

1

1 reference

25 July 2017

Ana Blanco

2

1 reference

25 July 2017

Ana Fernández-Marmiesse

3

1 reference

25 July 2017

Vanesa Alvarez-Iglesias

4

1 reference

25 July 2017

Clara Ruíz-Ponte

5

1 reference

25 July 2017

Ana Vega

7

1 reference

25 July 2017

29 June 2007

1 reference

25 July 2017

1 reference

25 July 2017

8

1 reference

25 July 2017

40

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-8-40

25 July 2017

0 references

cites work

Results of the 2003-2004 GEP-ISFG collaborative study on mitochondrial DNA: focus on the mtDNA profile of a mixed semen-saliva stain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

The R71G BRCA1 is a founder Spanish mutation and leads to aberrant splicing of the transcript

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

Evidence of founder mutations in Finnish BRCA1 and BRCA2 families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects.

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2350-8-40

Typing of mitochondrial DNA coding region SNPs of forensic and anthropological interest using SNaPshot minisequencing.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2350-8-40

High proportion of BRCA1/2 founder mutations in Hispanic breast/ovarian cancer families from Colombia.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1924843

Coding region mitochondrial DNA SNPs: Targeting East Asian and Native American haplogroups

31 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2350-8-40

Multiplex single-nucleotide primer extension analysis to simultaneously detect eleven BRCA1 mutations in breast cancer families

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17603881

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

BRCA1 and BRCA2 mutations in a South American population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17603881

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Analysis of BRCA1 and BRCA2 in breast and breast/ovarian cancer families shows population substructure in the Iberian peninsula

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17603881

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-8-40

1 reference

Dimensions Publication ID

25 July 2017

0 references

1 reference

25 July 2017

1 reference