Prenatal karyotyping was performed on 136 patients because of one or m
ore abnormalities detected on ultrasound, A total of 188 specimens was
obtained which included fetal blood, amniotic fluid and chorionic vil
lus, In 52 patients a second or 'backup' sample was obtained and in 10
0% cytogenetic analysis was successful. In contrast, failure to obtain
a result occurred in 4 (4.7%) of the remaining 84 patients where a se
cond sample was not obtained. In the event of primary sample failure,
backup sampling not only improves the karyotype yield, but obviates th
e need for a second pass procedure with its attendant risks.