(Q25257213)

6 July 2017

title

The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations (English)

1 reference

6 July 2017

1 reference

William David Foulkes

object named as

William D Foulkes

8

0 references

Frans Hogervorst

4

object named as

Frans Hogervorst

1 reference

6 July 2017

6

Pål Møller

1 reference

6 July 2017

Teresa M Rudkin

1

1 reference

6 July 2017

Nancy Hamel

2

1 reference

6 July 2017

Maria Galvez

3

1 reference

6 July 2017

Johan J P Gille

5

1 reference

6 July 2017

Jaran Apold

7

1 reference

6 July 2017

language of work or name

English

0 references

publication date

1 March 2006

1 reference

6 July 2017

1 reference

6 July 2017

volume

7

1 reference

6 July 2017

issue

1

0 references

page(s)

15

1 reference

Identification of a founder BRCA2 mutation in Sardinia

6 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1403746

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1403746

BRCA1 mutations in Ashkenazi Jewish women

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1403746

A high proportion of founder BRCA1 mutations in Polish breast cancer families

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1403746

The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1403746

Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1403746

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1403746

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1403746

Mutation analysis of the BRCA1 gene in 23 families with cases of cancer of the breast, ovary, and multiple other sites

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1403746

The BRCA1 syndrome and other inherited breast or breast-ovarian cancers in a Norwegian prospective series

28 September 2017

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-15

Genetic epidemiology of BRCA1 mutations in Norway.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-15

Three per cent of Norwegian Ovarian Cancers are caused by BRCA1 1675delA or 1135insA

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-15

Haplotype Analysis of BRCA2 8765delAG Mutation Carriers in French Canadian and Yemenite Jewish Hereditary Breast Cancer Families

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-15

21 January 2018

Identifiers

DOI

10.1186/1471-2350-7-15

1 reference

Dimensions Publication ID

6 July 2017

0 references

1 reference

6 July 2017

1 reference