How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies

Exome sequencing (ES) enhanced the diagnostic yield of genetic testing, but has also increased the possibility of uncertain findings. Prenatal ES is increasingly being offered after a fetal abnormality is detected through ultrasound. It is important to know how to handle uncertainty in this particul...

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Detalles Bibliográficos
Autores principales: Klapwijk, Jasmijn E., Srebniak, Malgorzata I., Go, Attie T. J. I., Govaerts, Lutgarde C. P., Lewis, Celine, Hammond, Jennifer, Hill, Melissa, Lou, Stina, Vogel, Ida, Ormond, Kelly E., Diderich, Karin E. M., Brüggenwirth, Hennie T., Riedijk, Sam R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2021
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596644/
https://www.ncbi.nlm.nih.gov/pubmed/34155632
http://dx.doi.org/10.1111/cge.14010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596644/
https://www.ncbi.nlm.nih.gov/pubmed/34155632
http://dx.doi.org/10.1111/cge.14010

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