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. Author manuscript; available in PMC: 2018 Mar 9.
Published before final editing as: Arch Pathol Lab Med. 2016 Sep 9:10.5858/arpa.2016-0156-RA. doi: 10.5858/arpa.2016-0156-RA

Figure 8.

Figure 8

Schematic representation of the “double-cut” methodology, in which multiple sequential levels of a single specimen are placed onto a fluorescence in situ hybridization–compatible slide such that all tumor cells are under a single hybridization area (hematoxylin-eosin, original magnifications ~×20 [left] and ~×200 [right]).