We report on the prenatal diagnosis of a fetus with 46,XY and 46,XX cell li
nes with a normal male phenotype, Cytogenetic and molecular studies ruled o
ut the possibility of maternal cell contamination and showed that all the X
chromosomes present in both fetal cell lines were derived from a single ma
ternal X chromosome, This suggests 46,XY/46,XX mosaicism. (C) 1999 Wiley-Li
ss, Inc.