Prenatal detection of fetal Down's syndrome from maternal plasma
- PMID: 11117917
- DOI: 10.1016/s0140-6736(00)03237-2
Prenatal detection of fetal Down's syndrome from maternal plasma
Abstract
Fetal DNA is present in maternal plasma, and a proportion of such DNA is seen in intact fetal cells. We investigated the use of fluorescence in-situ hybridisation (FISH) techniques on maternal plasma samples. In plasma samples obtained from three women carrying fetuses affected by trisomy 21 (Down's syndrome), we identified fetal cells with three chromosome-21 signals. These results show the feasibility of non-invasive detection of fetal chromosomal aneuploidy by maternal plasma analysis.
Comment in
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Prenatal detection of fetal Down's syndrome.Lancet. 2001 Mar 24;357(9260):958-9. doi: 10.1016/S0140-6736(05)71658-5. Lancet. 2001. PMID: 11289373 No abstract available.
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Non-invasive prenatal diagnosis of Down's syndrome.Lancet. 2001 Mar 24;357(9260):963-4. doi: 10.1016/S0140-6736(05)71670-6. Lancet. 2001. PMID: 11289381 No abstract available.
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