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

Overview of attention for article published in Hereditary Cancer in Clinical Practice, June 2016

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Among the highest-scoring outputs from this source (#49 of 260)
Good Attention Score compared to outputs of the same age (71st percentile)
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Implications of using genome sequencing to test unselected populations for BRCA1/2 variants: a modelling study https://t.co/0HcUJlA7Tw

RT @DrKhouryCDC: Should genome sequencing be used in population screening for high risk breast cancer genes? https://t.co/XxbfRxPNYK https:…

RT @DrKhouryCDC: Should genome sequencing be used in population screening for high risk breast cancer genes? https://t.co/XxbfRxPNYK https:…

RT @DrKhouryCDC: Should genome sequencing be used in population screening for high risk breast cancer genes? https://t.co/XxbfRxPNYK https:…

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