Identification of germline 185delAG BRCA1 mutations in non-Jewish Americans of Spanish ancestry from the San Luis Valley, Colorado (Q35184354)

7 August 2017

1 reference

title

Identification of germline 185delAG BRCA1 mutations in non-Jewish Americans of Spanish ancestry from the San Luis Valley, Colorado. (English)

1 reference

7 August 2017

Lisa G Mullineaux

1 reference

7 August 2017

Teresa M Castellano

1 reference

7 August 2017

Jeffrey Shaw

1 reference

7 August 2017

Lisen Axell

1 reference

7 August 2017

Marie E Wood

1 reference

7 August 2017

Sami Diab

1 reference

7 August 2017

Catherine Klein

1 reference

7 August 2017

Mark Sitarik

1 reference

7 August 2017

Amie M Deffenbaugh

1 reference

7 August 2017

Sharon L Graw

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 August 2003

1 reference

7 August 2017

1 reference

7 August 2017

1 reference

7 August 2017

1 reference

7 August 2017

page(s)

597-602

1 reference

The genetic attributable risk of breast and ovarian cancer

7 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Cancer Risk Estimates for BRCA1 Mutation Carriers Identified in a Risk Evaluation Program

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Cancer Incidence in BRCA1 mutation carriers

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Unusual case of Smith-Lemli-Opitz syndrome "type II"

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Cancer risks in BRCA2 mutation carriers

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Cancer Risks in Two Large Breast Cancer Families Linked to BRCA2 on Chromosome 13q12‐13

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

The 185delAG BRCA1 mutation originated before the dispersion of Jews in the diaspora and is not limited to Ashkenazim

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

BRCA1 185delAG mutation in a non-Ashkenazi Jewish woman with early-onset breast and ovarian cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Prevalence of BRCA1 and BRCA2 Jewish mutations in Spanish breast cancer patients.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

BRCA1 mutation analysis in 83 Spanish breast and breast/ovarian cancer families

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Two contiguously located germline BRCA1 mutations in a Spanish early-onset breast cancer family

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Molecular analysis of the six most recurrent mutations in the BRCA1 gene in 87 Spanish breast/ovarian cancer families

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Mutation analysis of the BRCA2 gene in breast/ovarian cancer Spanish families: identification of two new mutations

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Spanish family study on hereditary breast and/or ovarian cancer: Analysis of theBRCA1 gene

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Association between BRCA1 and BRCA2 mutations and cancer phenotype in Spanish breast/ovarian cancer families: implications for genetic testing

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Frequency of germ-line BRCA1 mutations among Spanish families from a Mediterranean area

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Statement of the American Society of Clinical Oncology: genetic testing for cancer susceptibility, Adopted on February 20, 1996

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Niemann-Pick C1 disease: the I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotype

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Natural history of the recombinant (8) syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Cloning, sequencing, and analysis of inv8 chromosome breakpoints associated with recombinant 8 syndrome

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Major histocompatibility complex haplotype studies in Ashkenazi Jewish patients with pemphigus vulgaris

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Identification of the 185delAG BRCA1 mutation in a Spanish Gypsy population

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

BRCA2 mutation analysis of 87 Spanish breast/ovarian cancer families

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.11533

7 January 2021

Identifiers

DOI

10.1002/CNCR.11533

1 reference

7 August 2017

1 reference