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d Two-color FISH assay results.
Results were 100% concordant with FISH assay results.
A deletion of 5′RET was revealed by FISH assay, indicating RET-gene rearrangement.
This FISH assay is useful for diagnostic screening of NUP98-positive leukemias.
In addition, an Ewing sarcoma breakpoint region 1 gene, 22q12 rearrangement was proven by a two-color fluorescence in situ hybridization (FISH) assay (Fig. 4d).
When the FISH assay was applied to five normal and five inversion male samples, the correct genotype was assignable with p < 0.001 for all samples.
We designed a specific double-color double-fusion FISH assay to discriminate between this t(11 12)(p15 q13) and those producing NUP98-HOXC11 or NUP98-HOXC13 NUP98-HOXC13
The FISH assay described here enables simultaneous location and molecular identification of T. foetus in formalin-fixed and paraffin-embedded histological specimens of intestinal trichomonosis.
For FISH assay, cells were treated as described previously [3].
We are grateful to Liz Chavez from University of British Columbia for her assistance in the telomere FISH assay.
We sought to determine whether a HER2 FISH assay could be reliably used to detect HER2 amplification in CTCs.
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