Evaluating parents’ decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol

BACKGROUND: Using next-generation sequencing (NGS) in newborn screening (NBS) could expand the number of genetic conditions detected pre-symptomatically, simultaneously challenging current precedents, raising ethical concerns, and extending the role of parental decision-making in NBS. The NC NEXUS (...

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Detalles Bibliográficos
Autores principales: Milko, Laura V., Rini, Christine, Lewis, Megan A., Butterfield, Rita M., Lin, Feng-Chang, Paquin, Ryan S., Powell, Bradford C., Roche, Myra I., Souris, Katherine J., Bailey, Donald B., Berg, Jonathan S., Powell, Cynthia M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Study Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022715/
https://www.ncbi.nlm.nih.gov/pubmed/29950170
http://dx.doi.org/10.1186/s13063-018-2686-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022715/
https://www.ncbi.nlm.nih.gov/pubmed/29950170
http://dx.doi.org/10.1186/s13063-018-2686-4

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