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Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma
Current prenatal diagnosis for fetal aneuploidies (including trisomy 21 [T21]) generally relies on an initial biochemical serum-based noninvasive prenatal testing (NIPT) after which women who are deemed to be at high risk are offered an invasive confirmatory test (amniocentesis or chorionic villi sa...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove Medical Press
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4104725/ https://ncbi.nlm.nih.gov/pubmed/25053891 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S35602 |
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