Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma

Chromosomal aneuploidy is the major reason why couples opt for prenatal diagnosis. Current methods for definitive diagnosis rely on invasive procedures, such as chorionic villus sampling and amniocentesis, and are associated with a risk of fetal miscarriage. Fetal DNA has been found in maternal plas...

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Bibliografiska uppgifter
Huvudupphovsmän: Chiu, Rossa W. K., Chan, K. C. Allen, Gao, Yuan, Lau, Virginia Y. M., Zheng, Wenli, Leung, Tak Y., Foo, Chris H. F., Xie, Bin, Tsui, Nancy B. Y., Lun, Fiona M. F., Zee, Benny C. Y., Lau, Tze K., Cantor, Charles R., Lo, Y. M. Dennis
Materialtyp: Artigo
Språk:Inglês
Publicerad: National Academy of Sciences 2008
Ämnen:
Biological Sciences
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2600580/
https://ncbi.nlm.nih.gov/pubmed/19073917
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0810641105
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