Abstract
CHROMOSOME analysis can be performed on fibroblasts cultured from amniotic fluid1–3. This is the basis of a technique for the intrauterine detection of chromosomal aberrations in the foetuses of women who are known to have a high risk of producing abnormal offspring. Valenti et al.1, for example, reported the intrauterine detection of trisomy 21 in amniotic fluid cell cultures and they subsequently performed a therapeutic abortion. The pathological findings on the foetus confirmed the diagnosis.
Similar content being viewed by others
References
Valenti, C., Schutta, E. J., and Kehaty, T., Lancet, ii, 220 (1968).
Steele, M. W., and Breg, jun., W. R., Lancet, i, 383 (1966).
Nadler, H. L., Pediatrics, 42, 912 (1968).
Lancet, ii, 89 (1969).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
LISGAR, F., GERTNER, M., CHERRY, S. et al. Prenatal Chromosome Analysis. Nature 225, 280–281 (1970). https://doi.org/10.1038/225280a0
Received:
Issue Date:
DOI: https://doi.org/10.1038/225280a0
- Springer Nature Limited
This article is cited by
-
Pr�natale Chromosomenanalyse mit Mosaikbefund 46,XX/92,XXXX
Human Genetics (1971)
-
Prenatal genetic diagnosis
La Ricerca in Clinica e in Laboratorio (1971)