(Q36620818)

15 August 2017

Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families (English)

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15 August 2017

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11

Devilee P

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15 August 2017

8

Stratton M

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15 August 2017

Hanne Meijers-Heijboer

7

object named as

Meijers-Heijboer H

1 reference

15 August 2017

5

Vasen HF

1 reference

15 August 2017

Peelen T

1

1 reference

15 August 2017

van Vliet M

2

1 reference

15 August 2017

Bosch A

3

1 reference

15 August 2017

Bignell G

4

1 reference

15 August 2017

Klijn JG

6

1 reference

15 August 2017

van Ommen GJ

9

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15 August 2017

Cornelisse CJ

10

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15 August 2017

language of work or name

English

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publication date

1 January 2000

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British Journal of Cancer

15 August 2017

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15 August 2017

82

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15 August 2017

1

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15 August 2017

151-156

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https://scigraph.springernature.com/pub.10.1054/bjoc.1999.0892

15 August 2017

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cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

A low proportion of BRCA2 mutations in Finnish breast cancer families.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

Mutation analysis in the BRCA2 gene in primary breast cancers

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

BRCA2 mutations in primary breast and ovarian cancers

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

A simple salting out procedure for extracting DNA from human nucleated cells

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

Analysis of BRCA1 and BRCA2 mutations in Hungarian families with breast or breast-ovarian cancer

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

BRCA2 mutations in hereditary breast and ovarian cancer in France

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

Population genetics of BRCA1 and BRCA2.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation?

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

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

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

THE GENETICS OF BREAST CANCER SUSCEPTIBILITY

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363204

Rapid detection of BRCA1 mutations by the protein truncation test

4 December 2018

1 reference

12 December 2020

The majority of 22 Dutch high-risk breast cancer families are due to either BRCA1 or 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

A 1-kb Alu-mediated germ-line deletion removing BRCA1 exon 17

1 reference

12 December 2020

A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family

1 reference

12 December 2020

Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions

1 reference

12 December 2020

Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer

1 reference

12 December 2020

Identifiers

DOI

10.1054/BJOC.1999.0892

1 reference

Dimensions Publication ID

15 August 2017

0 references

1 reference

15 August 2017

PubMed publication ID

10638982

1 reference