Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.

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Effects of Endocrine-Disrupting Chemicals and Epigenetic Modifications in Ovarian Cancer: A Review.Changes in classification of genetic variants in BRCA1 and BRCA2.

P2860

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P2860

Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.

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http://www.wikidata.org/entity/Q48096924

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

@wuu

2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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name

Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.

@en

Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.

@nl

type

Item

label

Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.

@en

Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.

@nl

prefLabel

Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.

@en

Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.

@nl

P1476

Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.

@en

P2093

Andreas Rump

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Carolin Eva Sadowski

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Cornelia Meisel

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Daniela Kohlstedt

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Evelin Schröck

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Franziska Stäritz

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Karin Kast

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Katja Keller

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Kerstin Becker

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

Luisa Mackenroth

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P2860

KRAS mutations as an independent prognostic factor in patients with advanced colorectal cancer treated with cetuximab.

Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.

Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

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

Association of BRCA2 N372H polymorphism with cancer susceptibility: a comprehensive review and meta-analysis.

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 performance of BRCA1 immunohistochemistry for detecting germline, somatic, and epigenetic BRCA1 loss in high-grade serous ovarian cancer.

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results.

ENIGMA--evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes

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s00404-017-4330-z

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1227-1238

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scholarly article

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10.1007/S00404-017-4330-Z

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295

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Norbert Arnold

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2017-03-21T00:00:00Z

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28324225

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Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.

about

P2860

P2860

Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study.

description

name

type

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prefLabel

P1433

P1476

P2093

P2860

P2888

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P433

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P50

P577

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P356

P1433

P1476

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P2860

P2888

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P356

P433

P478

P50

P577

P698