Anomalous PCR products are often produced during the amplification of
d(CA)n . d(TG)n sequences. Upon denaturing polyacrylamide gel electrop
horesis, these products yield a ladder-like pattern that can complicat
e genotypic interpretation. We have developed two related techniques,
referred to as two- and three-stage linear amplification (2-SLA and 3-
SLA, respectively), which largely overcome this problem and yield read
ily interpretable banding patterns.