The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations - Wikidata - awgldk - TriplyDB

The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations

The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations

http://www.wikidata.org/entity/Q25257213

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Hereditary breast cancer in Middle Eastern and North African (MENA) populations: identification of novel, recurrent and founder BRCA1 mutations in the Tunisian population Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control.The relative contribution of point mutations and genomic rearrangements in BRCA1 and BRCA2 in high-risk breast cancer families.Reconstructing the genealogy of a BRCA1 founder mutation by phylogenetic analysis.A founder BRCA2 mutation in non-Afrikaner breast cancer patients of the Western Cape of South Africa.Allelic imbalance in BRCA1 and BRCA2 gene expression is associated with an increased breast cancer risk.

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P2860

The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations

http://www.wikidata.org/entity/Q25257213

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2006 nî lūn-bûn

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2006 թուականի Մարտին հրատարակուած գիտական յօդուած

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2006 թվականի մարտին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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name

The frequent BRCA1 mutation 11 ...... study in different populations

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The frequent BRCA1 mutation 11 ...... study in different populations

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The frequent BRCA1 mutation 11 ...... study in different populations

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The frequent BRCA1 mutation 11 ...... study in different populations

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The frequent BRCA1 mutation 11 ...... study in different populations

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The frequent BRCA1 mutation 11 ...... study in different populations

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The frequent BRCA1 mutation 11 ...... study in different populations

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The frequent BRCA1 mutation 11 ...... study in different populations

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BMC Medical Genetics

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The frequent BRCA1 mutation 11 ...... study in different populations

@en

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Frans Hogervorst

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Jaran Apold

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Johan J P Gille

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Maria Galvez

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Nancy Hamel

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Pål Møller

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Teresa M Rudkin

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P2860

Identification of a founder BRCA2 mutation in Sardinia

BRCA1 mutations in Ashkenazi Jewish women

A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

Mutation analysis of the BRCA1 gene in 23 families with cases of cancer of the breast, ovary, and multiple other sites

The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer.

Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families.

Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.

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

A high proportion of founder BRCA1 mutations in Polish breast cancer families.

The BRCA1 syndrome and other inherited breast or breast-ovarian cancers in a Norwegian prospective series.

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15

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scholarly article

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10.1186/1471-2350-7-15

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1

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7

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William D Foulkes

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2006-03-01T00:00:00Z

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7267825

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16509964

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1403746

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