(Q35881432)

10 August 2017

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

1 reference

10 August 2017

1 reference

Dominique Stoppa-Lyonnet

22

object named as

D Stoppa-Lyonnet

0 references

Susan L Neuhausen

1

object named as

S L Neuhausen

1 reference

10 August 2017

13

F Couch

1 reference

10 August 2017

23

D Easton

1 reference

10 August 2017

4

M Stratton

1 reference

10 August 2017

Maria Adelaide Caligo

6

object named as

A Caligo

1 reference

10 August 2017

5

K Offit

1 reference

10 August 2017

17

S Narod

1 reference

10 August 2017

0 references

11

E Solomon

1 reference

10 August 2017

25

D E Goldgar

1 reference

10 August 2017

2

S Mazoyer

1 reference

10 August 2017

8

L Cannon-Albright

1 reference

10 August 2017

9

T Bishop

1 reference

10 August 2017

L Friedman

3

1 reference

10 August 2017

G Tomlinson

7

1 reference

10 August 2017

D Kelsell

10

1 reference

10 August 2017

B Weber

12

1 reference

10 August 2017

J Struewing

14

1 reference

10 August 2017

P Tonin

15

1 reference

10 August 2017

F Durocher

16

1 reference

10 August 2017

M H Skolnick

18

1 reference

10 August 2017

G Lenoir

19

1 reference

10 August 2017

O Serova

20

1 reference

10 August 2017

B Ponder

21

1 reference

10 August 2017

M C King

24

1 reference

10 August 2017

language of work or name

English

0 references

publication date

1 February 1996

1 reference

American Journal of Human Genetics

10 August 2017

1 reference

10 August 2017

58

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10 August 2017

2

1 reference

10 August 2017

271-280

1 reference

Mutation of human short tandem repeats

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Likelihood methods for locating disease genes in nonequilibrium populations.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Haplotypes and mutations in Wilson disease.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

BRCA1 mutations in Ashkenazi Jewish women

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Mutation and cancer: statistical study of retinoblastoma

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914544

Familial breast-ovarian cancer locus on chromosome 17q12-q23

27 July 2018

1 reference

12 December 2020

Haplotype analysis to determine the position of a mutation among closely linked DNA markers

1 reference

12 December 2020

A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening

1 reference

12 December 2020

A P1-based physical map of the region from D17S776 to D17S78 containing the breast cancer susceptibility gene BRCA1

1 reference

12 December 2020

Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer

1 reference

12 December 2020

Rapid detection of BRCA1 mutations by the protein truncation test

1 reference

12 December 2020

Identifiers

1 reference

10 August 2017

PubMed publication ID

8571953

1 reference