(Q34385784)

1 August 2017

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

1 reference

1 August 2017

1 reference

Dominique Stoppa-Lyonnet

6

D Stoppa-Lyonnet

0 references

Ana Osorio

11

A Osorio

1 reference

1 August 2017

T Bishop

21

0 references

Susan L Neuhausen

1

S L Neuhausen

1 reference

1 August 2017

22

D Easton

1 reference

1 August 2017

27

P Devilee

1 reference

1 August 2017

23

J Benitez

1 reference

1 August 2017

12

M Stratton

1 reference

1 August 2017

Maria Adelaide Caligo

15

M A Caligo

1 reference

1 August 2017

29

S A Narod

1 reference

1 August 2017

13

K Offit

1 reference

1 August 2017

20

L Cannon-Albright

1 reference

1 August 2017

5

J Garber

1 reference

1 August 2017

A K Godwin

2

1 reference

1 August 2017

R Gershoni-Baruch

3

1 reference

1 August 2017

E Schubert

4

1 reference

1 August 2017

E Olah

7

1 reference

1 August 2017

B Csokay

8

1 reference

1 August 2017

O Serova

9

1 reference

1 August 2017

F Lalloo

10

1 reference

1 August 2017

J Boyd

14

1 reference

1 August 2017

R J Scott

16

1 reference

1 August 2017

A Schofield

17

1 reference

1 August 2017

E Teugels

18

1 reference

1 August 2017

M Schwab

19

1 reference

1 August 2017

M C King

24

1 reference

1 August 2017

B A Ponder

25

1 reference

1 August 2017

B Weber

26

1 reference

1 August 2017

A Borg

28

1 reference

1 August 2017

D Goldgar

30

1 reference

1 August 2017

language of work or name

English

0 references

publication date

1 June 1998

1 reference

American Journal of Human Genetics

1 August 2017

1 reference

1 August 2017

62

1 reference

1 August 2017

1381-1388

1 reference

1 August 2017

6

1 reference

Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

Population genetics of BRCA1 and BRCA2.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

Generation of an integrated transcription map of the BRCA2 region on chromosome 13q12-q13

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

A comprehensive genetic map of the human genome based on 5,264 microsatellites

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

Identification of the breast cancer susceptibility gene BRCA2

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

Could the 185delAG BRCA1 mutation be an ancient Jewish mutation?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

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

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377164

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

9 December 2018

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

Breast cancer and BRCA1 mutations

1 reference

12 December 2020

Germline BRCA1 185delAG mutations in Jewish women with breast cancer

1 reference

12 December 2020

Identifiers

DOI

10.1086/301885

1 reference

1 August 2017

1 reference

1 August 2017

1 reference