Next-Generation Sequencing in Order to Better Characterize a BRCA Variant of Uncertain Significance

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Next-Generation Sequencing in Order to Better Characterize a BRCA Variant of Uncertain Significance

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Next-Generation Sequencing in ...... iant of Uncertain Significance

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Next-Generation Sequencing in ...... iant of Uncertain Significance

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Next-Generation Sequencing in ...... iant of Uncertain Significance

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P1476

Next-Generation Sequencing in ...... iant of Uncertain Significance

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P2093

Shakti Ramkissoon

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Steven Sorscher

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P2860

BRCA1 and BRCA2 and the genetics of breast and ovarian cancer.

Low incidence of BRCA2 mutations in breast carcinoma and other cancers.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

The Clinical Significance of Unknown Sequence Variants in BRCA Genes.

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017.

Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: variant reclassification and surgical decisions.

Loss of heterozygosity analysis at theBRCAloci in tumor samples from patients with familial breast cancer

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634-637

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scholarly article

case report

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10.1159/000478005

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P433

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P478

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2017-05-01T00:00:00Z

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P698

28868023

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P932

5566997

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