Cite
HARVARD Citation
Schreiber, E. et al. (n.d.). Confirming variants discovered by Next Generation Sequencing (NGS) with Sanger sequencing using innovative bioinformatics tools. European journal of cancer. pp. S19-. [Online].
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Schreiber, E. et al. (n.d.). Confirming variants discovered by Next Generation Sequencing (NGS) with Sanger sequencing using innovative bioinformatics tools. European journal of cancer. pp. S19-. [Online].