BRCA Share: A Collection of Clinical BRCA Gene Variants. - Test2 - elhamkhani - TriplyDB

BRCA Share: A Collection of Clinical BRCA Gene Variants.

BRCA Share: A Collection of Clinical BRCA Gene Variants.

http://www.wikidata.org/entity/Q39384483

about

Sharing Data to Build a Medical Information Commons: From Bermuda to the Global Alliance.Identification of differentially methylated BRCA1 and CRISP2 DNA regions as blood surrogate markers for cardiovascular disease Actionable Genes, Core Databases, and Locus-Specific Databases.The frequency of cancer predisposition gene mutations in hereditary breast and ovarian cancer patients in Taiwan: From BRCA1/2 to multi-gene panels.Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratory.HUMA: A platform for the analysis of genetic variation in humans.WES/WGS Reporting of Mutations from Cardiovascular "Actionable" Genes in Clinical Practice: A Key Role for UMD Knowledgebases in the Era of Big Databases.Identification of Eight Spliceogenic Variants in BRCA2 Exon 16 by Minigene Assays.Detecting Disease Specific Pathway Substructures through an Integrated Systems Biology Approach.A new bioinformatics tool to help assess the significance of BRCA1 variants.Association of with early age onset of breast cancer patients in selected cohort from Pakistani population

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P2860

BRCA Share: A Collection of Clinical BRCA Gene Variants.

http://www.wikidata.org/entity/Q39384483

description

2016 nî lūn-bûn

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2016年の論文

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2016年學術文章

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name

BRCA Share: A Collection of Clinical BRCA Gene Variants.

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BRCA Share: A Collection of Clinical BRCA Gene Variants.

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type

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BRCA Share: A Collection of Clinical BRCA Gene Variants.

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BRCA Share: A Collection of Clinical BRCA Gene Variants.

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BRCA Share: A Collection of Clinical BRCA Gene Variants.

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BRCA Share: A Collection of Clinical BRCA Gene Variants.

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BRCA Share: A Collection of Clinical BRCA Gene Variants.

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Alecia Willis

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Angela Love

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Brigitte Bressac-De Paillerets

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Camille R Nery

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Charles M Strom

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P2860

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

dbSNP: the NCBI database of genetic variation

A guide for functional analysis of BRCA1 variants of uncertain significance

Recent Enhancements to the Genetic Risk Prediction Model BRCAPRO

Linkage of early-onset familial breast cancer to chromosome 17q21

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium

The Matchmaker Exchange: a platform for rare disease gene discovery

Cancer incidence and mortality patterns in Europe: estimates for 40 countries in 2012

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

The breast cancer information core: database design, structure, and scope.

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