Persistent problems with false positive results were encountered when carry
ing out a published RT-PCR method to detect the CBF beta/MYH11 transcripts
associated with the inv(16)(p13q22) cytogenetic abnormality in acute myeloi
d leukaemia. These were shown to be due to amplification of part of the int
ronic MYH11 sequence, presumably from very small amounts of contaminating D
NA or unspliced primary RNA transcripts, amplified because of partial homol
ogy of the CBF beta 3 primer to intronic MYH11 sequence.