Study of a single BRCA2 mutation with high carrier frequency in a small population - Wikidata - wikimedia - TriplyDB

Study of a single BRCA2 mutation with high carrier frequency in a small population

Study of a single BRCA2 mutation with high carrier frequency in a small population

http://www.wikidata.org/entity/Q24680535

about

Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear family Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer Founder populations and their uses for breast cancer genetics.Evidence of a founder BRCA1 mutation in Scotland BRCA1 and BRCA2 mutations in Scotland and Northern Ireland BRCA2 mutation carriers, reproductive factors and breast cancer risk The Icelandic founder mutation BRCA2 999del5: analysis of expression Optimal delivery of male breast cancer follow-up care: improving outcomes Male breast cancer in Cowden syndrome patients with germline PTEN mutations BRCA1 and BRCA2 testing: weighing the demand against the benefits.Association of Cancer Incidence and Duration of Residence in Geothermal Heating Area in Iceland: An Extended Follow-Up The BARD1 Cys557Ser variant and breast cancer risk in Iceland A population study of mutations and LOH at breast cancer gene loci in tumours from sister pairs: two recurrent mutations seem to account for all BRCA1/BRCA2 linked breast cancer in Iceland.Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer.Variation in cancer risks, by mutation position, in BRCA2 mutation carriers.Family history of cancer and risk of pancreatic cancer: a pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan).Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families.Mutations in BRCA2 and PALB2 in male breast cancer cases from the United States Identification of a new BRCA2 large genomic deletion associated with high risk male breast cancer Old meets new: identifying founder mutations in genetic disease.CpG island hypermethylation of BRCA1 and loss of pRb as co-occurring events in basal/triple-negative breast cancer.Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers Breast cancer incidence and familiality in Iceland during 75 years from 1921 to 1995 The effect of a single BRCA2 mutation on cancer in Iceland CDKN2A mutations and melanoma risk in the Icelandic population.Anticipation in familial pancreatic cancer.Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas.Do Breast Cancer Patients Tested in the Oncology Care Setting Share BRCA Mutation Results with Family Members and Health Care Providers?Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control.A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers.BRCA1 mutations in southern England High prevalence of BRCA1 stop mutation c.4183C>T in the Tyrolean population: implications for genetic testing An inherited NBN mutation is associated with poor prognosis prostate cancer The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions.The rate of the 6174delT founder Jewish mutation in BRCA2 in patients with non-colonic gastrointestinal tract tumours in Israel.CYP17 promoter polymorphism and breast cancer risk in males and females in relation to BRCA2 status Similar prevalence of founder BRCA1 and BRCA2 mutations among Ashkenazi and non-Ashkenazi men with breast cancer: evidence from 261 cases in Israel, 1976-1999.Aurora A is a prognostic marker for breast cancer arising in BRCA2 mutation carriers.The role of the BRCA2 gene in susceptibility to prostate cancer revisited A personalised approach to prostate cancer screening based on genotyping of risk founder alleles

P2860

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P2860

Study of a single BRCA2 mutation with high carrier frequency in a small population

http://www.wikidata.org/entity/Q24680535

description

1997 nî lūn-bûn

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1997 թուականի Մայիսին հրատարակուած գիտական յօդուած

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1997 թվականի մայիսին հրատարակված գիտական հոդված

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1997年の論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年论文

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name

Study of a single BRCA2 mutation with high carrier frequency in a small population

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Study of a single BRCA2 mutation with high carrier frequency in a small population

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Study of a single BRCA2 mutation with high carrier frequency in a small population

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type

label

Study of a single BRCA2 mutation with high carrier frequency in a small population

@ast

Study of a single BRCA2 mutation with high carrier frequency in a small population

@en

Study of a single BRCA2 mutation with high carrier frequency in a small population

@nl

prefLabel

Study of a single BRCA2 mutation with high carrier frequency in a small population

@ast

Study of a single BRCA2 mutation with high carrier frequency in a small population

@en

Study of a single BRCA2 mutation with high carrier frequency in a small population

@nl

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American Journal of Human Genetics

P1476

Study of a single BRCA2 mutation with high carrier frequency in a small population

@en

P2093

G Olafsdottir

http://www.w3.org/2001/XMLSchema#string

H Bjarnadottir

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H Tulinius

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J E Eyfjörd

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J G Jonasson

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L Tryggvadottir

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S Sigurdsson

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S Thorlacius

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P2860

Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium

Identification of the breast cancer susceptibility gene BRCA2

Identification by representational difference analysis of a homozygous deletion in pancreatic carcinoma that lies within the BRCA2 region.

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

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

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

The genetics of breast and ovarian cancer

Estrogens, progestogens, normal breast cell proliferation, and breast cancer risk.

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

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

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1079-84

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1483789

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5

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60

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9150155

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1712443

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