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Three years of clinical experience with a genome-wide cfDNA screening test for aneuploidies and copy-number variants
PURPOSE: Pregnant women have unprecedented choices for prenatal screening and testing. Cell-free DNA (cfDNA) offers the option to screen for aneuploidy of all chromosomes and genome-wide copy-number variants (CNVs), expanding screening beyond the common trisomies (“traditional” cfDNA). We sought to...
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| Publicado no: | Genet Med |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group US
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8257487/ https://ncbi.nlm.nih.gov/pubmed/33731879 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41436-021-01135-8 |
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