Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling study

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Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling study

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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Implications of using whole ge ...... ancer genes: a modelling study

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Implications of using whole ge ...... ancer genes: a modelling study

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Implications of using whole ge ...... ancer genes: a modelling study

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P1476

Implications of using whole ge ...... ancer genes: a modelling study

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P2093

Hilary Burton

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Mark Kroese

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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

Meta-analysis of BRCA1 and BRCA2 penetrance

Recommendations for returning genomic incidental findings? We need to talk!

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.

Not-so-incidental findings: the ACMG recommendations on the reporting of incidental findings in clinical whole genome and whole exome sequencing

ACMG clinical laboratory standards for next-generation sequencing.

Clinical interpretation and implications of whole-genome sequencing.

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s13053-016-0052-7

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scholarly article

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10.1186/S13053-016-0052-7

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Charlotte Warren-Gash

Paul D P Pharoah

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2016-06-01T00:00:00Z

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1018958697

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27252788

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4888520

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