Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children
- PMID: 34166672
- DOI: 10.1016/j.jpeds.2021.06.042
Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children
Comment in
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Implementing Rapid Whole-Genome Sequencing in Critical Care: A Qualitative Study of Facilitators and Barriers to New Technology Adoption.J Pediatr. 2021 Oct;237:237-243.e2. doi: 10.1016/j.jpeds.2021.05.045. Epub 2021 May 21. J Pediatr. 2021. PMID: 34023348
Comment on
-
Implementing Rapid Whole-Genome Sequencing in Critical Care: A Qualitative Study of Facilitators and Barriers to New Technology Adoption.J Pediatr. 2021 Oct;237:237-243.e2. doi: 10.1016/j.jpeds.2021.05.045. Epub 2021 May 21. J Pediatr. 2021. PMID: 34023348
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