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. 2011 Jan;13(1):85–92. doi: 10.1016/j.jmoldx.2010.11.004

Figure 1.

Figure 1

Primer design for detection of BCL2-IGH translocation (A) and internal tandem deletion mutation of the FLT3 gene (B). Sizes are not to scale. Arrows indicate primers and lines indicates location of the probe for real-time PCR. The Δ indicates the defined size difference of the paired amplicons for each breakpoint and an asterisk indicates the segment of ITD mutation.