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Published in 2017 at "Experimental and molecular pathology"
DOI: 10.1016/j.yexmp.2017.03.001
Abstract: PURPOSE Conventional methods used to identify BRCA1/2 germline mutations in hereditary cancers are time-consuming and expensive, due to the large size of the genes. The recent introduction of next generation sequencing (NGS) benchtop platforms is…
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Keywords:
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