(Q27496673)

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Haplotype analysis suggest common founders in carriers of the recurrent BRCA2mutation, 3398delAAAAG, in French Canadian hereditary breast and/ovarian cancer families

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Haplotype analysis suggest common founders in carriers of the recurrent BRCA2mutation, 3398delAAAAG, in French Canadian hereditary breast and/ovarian cancer families (English)

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1 reference

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Anne-Marie Mes-Masson

6

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William David Foulkes

object named as

William D Foulkes

7

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author name string

Kathleen K Oros

1

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Guy Leblanc

2

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Suzanna L Arcand

3

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Zhen Shen

4

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Chantal Perret

5

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Parviz Ghadirian

8

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Diane Provencher

9

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Patricia N Tonin

10

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publication date

15 March 2006

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BMC Medical Genetics

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7

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1

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23

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The human genome browser at UCSC

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

20 March 2017

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

20 March 2017

Microsatellites: simple sequences with complex evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

20 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

20 March 2017

A comparison of bayesian methods for haplotype reconstruction from population genotype data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

7 April 2017

Fallopian tube and primary peritoneal carcinomas associated with BRCA mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

29 September 2017

Variation in cancer risks, by mutation position, in BRCA2 mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

29 September 2017

Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

29 September 2017

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=1464093

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

29 September 2017

Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

29 September 2017

Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464093

29 September 2017

Prevalence of founder BRCA1 and BRCA2 mutations in unselected French Canadian women with breast cancer.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-23

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-23

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-23

21 January 2018

Significant proportion of breast and/or ovarian cancer families of French Canadian descent harbor 1 of 5BRCA1 andBRCA2 mutations

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-23

21 January 2018

The genetic attributable risk of breast and ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16539696

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene. Breast Cancer Information Core

1 reference

https://pubmed.ncbi.nlm.nih.gov/16539696

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16539696

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FounderBRCA1 andBRCA2 mutations in early-onset French Canadian breast cancer cases unselected for family history

1 reference

https://pubmed.ncbi.nlm.nih.gov/16539696

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1186/1471-2350-7-23

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