Genomic newborn screening: public health policy considerations and recommendations

BACKGROUND: The use of genome-wide (whole genome or exome) sequencing for population-based newborn screening presents an opportunity to detect and treat or prevent many more serious early-onset health conditions than is possible today. METHODS: The Paediatric Task Team of the Global Alliance for Gen...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:BMC Med Genomics
Päätekijät: Friedman, Jan M., Cornel, Martina C., Goldenberg, Aaron J., Lister, Karla J., Sénécal, Karine, Vears, Danya F.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2017
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5320805/
https://ncbi.nlm.nih.gov/pubmed/28222731
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-017-0247-4
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