Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children.

Creator(s)

John Lantos, Children's Mercy HospitalFollow

Document Type

Editorial

Publication Date

10-2021

Identifier

DOI: 10.1016/j.jpeds.2021.06.042

Abstract

Comment in

• Implementing Rapid Whole-Genome Sequencing in Critical Care: A Qualitative Study of Facilitators and Barriers to New Technology Adoption. Franck LS, Kriz RM, Rego S, Garman K, Hobbs C, Dimmock D.J Pediatr. 2021 Oct;237:237-243.e2. doi: 10.1016/j.jpeds.2021.05.045. Epub 2021 May 21.PMID: 34023348

Comment on

• Implementing Rapid Whole-Genome Sequencing in Critical Care: A Qualitative Study of Facilitators and Barriers to New Technology Adoption. Franck LS, Kriz RM, Rego S, Garman K, Hobbs C, Dimmock D.J Pediatr. 2021 Oct;237:237-243.e2. doi: 10.1016/j.jpeds.2021.05.045. Epub 2021 May 21.PMID: 34023348

Journal Title

The Journal of pediatrics

Volume

237

First Page

13

Last Page

15

MeSH Keywords

Child; Chromosome Mapping; Critical Care; Humans; Rare Diseases; Technology; Whole Genome Sequencing

Keywords

Child; Chromosome Mapping; Critical Care; Humans; Rare Diseases; Technology; Whole Genome Sequencing

Recommended Citation

Lantos JD. Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children. J Pediatr. 2021;237:13-15. doi:10.1016/j.jpeds.2021.06.042