The Clinical Significance of Unknown Sequence Variants in BRCA Genes. - Test2 - elhamkhani - TriplyDB

The Clinical Significance of Unknown Sequence Variants in BRCA Genes.

The Clinical Significance of Unknown Sequence Variants in BRCA Genes.

http://www.wikidata.org/entity/Q37334266

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The challenge of comprehensive and consistent sequence variant interpretation between clinical laboratories.Clinically Significant Unclassified Variants in BRCA1 and BRCA2 Genes Among Korean Breast Cancer Patients.Comparison of Clinical Outcomes of BRCA1/2 Pathologic Mutation, Variants of Unknown Significance, or Wild Type Epithelial Ovarian Cancer Patients P.Arg82Leu von Hippel-Lindau (VHL) gene mutation among three members of a family with familial bilateral pheochromocytoma in India: molecular analysis and in silico characterization.Characterization of BRCA1 and BRCA2 variants in multi-ethnic Asian cohort from a Malaysian case-control study Commercial Opportunities and Ethical Pitfalls in Personalized Medicine: A Myriad of Reasons to Revisit the Myriad Genetics Saga.Next-Generation Sequencing in Order to Better Characterize a BRCA Variant of Uncertain Significance Screening of the BRCA1 gene in Brazilian patients with breast and/or ovarian cancer via high-resolution melting reaction analysis.Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid.

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The Clinical Significance of Unknown Sequence Variants in BRCA Genes.

http://www.wikidata.org/entity/Q37334266

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

@pt

bilimsel makale

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scientific article published on 10 September 2010

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

@cs

name

The Clinical Significance of Unknown Sequence Variants in BRCA Genes.

@en

The Clinical Significance of Unknown Sequence Variants in BRCA Genes.

@nl

type

label

The Clinical Significance of Unknown Sequence Variants in BRCA Genes.

@en

The Clinical Significance of Unknown Sequence Variants in BRCA Genes.

@nl

prefLabel

The Clinical Significance of Unknown Sequence Variants in BRCA Genes.

@en

The Clinical Significance of Unknown Sequence Variants in BRCA Genes.

@nl

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The Clinical Significance of Unknown Sequence Variants in BRCA Genes

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Antonio Russo

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Laura La Paglia

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Loredana Bruno

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Naomi Margarese

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Valentina Calò

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P2860

The clinical management of BRCA1 and BRCA2 mutation carriers

Binding and recognition in the assembly of an active BRCA1/BARD1 ubiquitin-ligase complex

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

The RING heterodimer BRCA1-BARD1 is a ubiquitin ligase inactivated by a breast cancer-derived mutation

Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2

Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation

Likelihood ratio tests for detecting positive selection and application to primate lysozyme evolution

Amino acid difference formula to help explain protein evolution

Identification of the breast cancer susceptibility gene BRCA2

Distinguishing homologous from analogous proteins

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1644-1660

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scholarly article

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10.3390/CANCERS2031644

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3

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2

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Francesca Di Gaudio

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2010-09-10T00:00:00Z

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258955024

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