
pmid: 4737074
Summary. Because of the high mortality of human XO embryos, it was questioned whether the single X in a proportion of cells was inactivated. If genetic inactivation of the single X in XO conceptuses was of significant importance for reduced viability and subsequent abortion, a proportion of cells grown from XO fetuses should carry an inactivated late-labelling X chromosome. This hypothesis was tested by autoradiography and analysis of the late DNA-labelling pattern of XO cells derived from a 15-week-old spontaneous human abortus. None of the analysed cells had a late-labelling X chromosome. Consequently, the XO cells from this aborted fetus were not different from XO cells from liveborn individuals.
Silver, DNA, Glucosephosphate Dehydrogenase, Embryo, Mammalian, Tritium, Abortion, Spontaneous, Mice, Fetus, Pregnancy, Animals, Autoradiography, Humans, Female, Sex Chromosome Aberrations, Thymidine
Silver, DNA, Glucosephosphate Dehydrogenase, Embryo, Mammalian, Tritium, Abortion, Spontaneous, Mice, Fetus, Pregnancy, Animals, Autoradiography, Humans, Female, Sex Chromosome Aberrations, Thymidine
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