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Noninvasive Detection of Fetal Subchromosome Abnormalities via Deep Sequencing of Maternal Plasma
The purpose of this study was to determine the deep sequencing and analytic conditions needed to detect fetal subchromosome abnormalities across the genome from a maternal blood sample. Cell-free (cf) DNA was isolated from the plasma of 11 pregnant women carrying fetuses with subchromosomal duplicat...
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| Auteurs principaux: | , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Elsevier
2013
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3567270/ https://ncbi.nlm.nih.gov/pubmed/23313373 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2012.12.006 |
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