Clinical experience across the fetal‐fraction spectrum of a non‐invasive prenatal screening approach with low test‐failure rate

OBJECTIVE: To describe our clinical experience across the entire range of fetal‐fraction (FF) measurements of a non‐invasive prenatal screen (NIPS) that uses whole‐ genome sequencing (WGS). METHODS: We analyzed retrospectively results from 58 105 singleton pregnancies that underwent NIPS on a custom...

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Detalles Bibliográficos
Autores principales: Hancock, S., Ben‐Shachar, R., Adusei, C., Oyolu, C. B., Evans, E. A., Kang, H. P., Haverty, C., Muzzey, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2020
Materias:
Original Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496885/
https://www.ncbi.nlm.nih.gov/pubmed/31671482
http://dx.doi.org/10.1002/uog.21904

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496885/
https://www.ncbi.nlm.nih.gov/pubmed/31671482
http://dx.doi.org/10.1002/uog.21904

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