(Q35789846)

English

A multi-exonic BRCA1 deletion identified in multiple families through single nucleotide polymorphism haplotype pair analysis and gene amplification with widely dispersed primer sets

scientific article published on February 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

A multi-exonic BRCA1 deletion identified in multiple families through single nucleotide polymorphism haplotype pair analysis and gene amplification with widely dispersed primer sets (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

author name string

Benjamin D Ward

1

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Brant C Hendrickson

2

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Thaddeus Judkins

3

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Amie M Deffenbaugh

4

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Benoît Leclair

5

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Brian E Ward

6

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Thomas Scholl

7

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

publication date

1 February 2005

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

The Journal of Molecular Diagnostics

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

139-142

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Application of haplotype pair analysis for the identification of hemizygous loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867506

12 July 2018

Functional analysis of BRCA1 C-terminal missense mutations identified in 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=1867506

12 July 2018

The BRCA1 C-terminal domain: structure and function.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867506

12 July 2018

The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations. The BRCA1 Exon 13 Duplication Screening Group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867506

12 July 2018

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=1867506

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867506

12 July 2018

BRCA1 protein products ... Functional motifs...

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867506

12 July 2018

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867506

12 July 2018

Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867506

25 September 2018

BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867506

25 September 2018

Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families

1 reference

https://pubmed.ncbi.nlm.nih.gov/15681486

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE ESTIMATION OF GENE FREQUENCIES IN A RANDOM-MATING POPULATION

1 reference

https://pubmed.ncbi.nlm.nih.gov/15681486

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Over-representation of two specific haplotypes among chromosomes harbouring BRCA1 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15681486

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Exon 13 Duplication in the BRCA1 Gene Is a Founder Mutation Present in Geographically Diverse Populations

1 reference

https://api.crossref.org/works/10.1016%2FS1525-1578%2810%2960020-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S1525-1578(10)60020-7

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

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