Identification of a founder BRCA2 mutation in Sardinia - Wikidata - awgldk - TriplyDB

Identification of a founder BRCA2 mutation in Sardinia

Identification of a founder BRCA2 mutation in Sardinia

http://www.wikidata.org/entity/Q24649532

about

The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations Origin and distribution of the BRCA2-8765delAG mutation in breast cancer A role of BRCA1 and BRCA2 germline mutations in breast cancer susceptibility within Sardinian population Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control.Definition of the role of chromosome 9p21 in sporadic melanoma through genetic analysis of primary tumours and their metastases. The Melanoma Cooperative Group.HER2-positive male breast cancer: an update.Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations.Microsatellite instability and mutation analysis of candidate genes in unselected sardinian patients with endometrial carcinoma

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P2860

Identification of a founder BRCA2 mutation in Sardinia

http://www.wikidata.org/entity/Q24649532

description

2000 nî lūn-bûn

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2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2000 թվականի փետրվարին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年论文

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Identification of a founder BRCA2 mutation in Sardinia

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Identification of a founder BRCA2 mutation in Sardinia

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Identification of a founder BRCA2 mutation in Sardinia

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Identification of a founder BRCA2 mutation in Sardinia

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Identification of a founder BRCA2 mutation in Sardinia

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Identification of a founder BRCA2 mutation in Sardinia

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Identification of a founder BRCA2 mutation in Sardinia

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Identification of a founder BRCA2 mutation in Sardinia

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Identification of a founder BRCA2 mutation in Sardinia

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British Journal of Cancer

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Identification of a founder BRCA2 mutation in Sardinia

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P2860

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

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

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

Identification of the breast cancer susceptibility gene BRCA2

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

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes.

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

The same beta-globin gene mutation is present on nine different beta-thalassemia chromosomes in a Sardinian population.

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

Genetic analysis of breast cancer in the cancer and steroid hormone study

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