Chromosomal analysis of amniotic cell culture revealed an extra euchromatic
band in the variable heterochromatin region 9q12, Cytogenetic analysis of
the fetus was compared with the chromosomes of the parents, Using different
cytogenetic banding techniques and fluorescence in situ hybridization with
specific DNA probes, the structural rearrangements involved were considere
d, The very rare variant proved to be familiar. Demonstrating the inheritan
ce of a normal individual supports the interpretation of the prenatal analy
sis of chromosome 9 as a variant without clinical relevance for the fetus.