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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: National Academy of Sciences 2008
Gaiak:
Biological Sciences
Sarrera elektronikoa: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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