Diagnosis Through Whole Genome Sequencing and Care Utilization in Children With Severe Illness.
- DOI
- 10.1001/jamanetworkopen.2026.34372
- Published
- 2026 Sep 1
- Container
- JAMA network open
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1001/jamanetworkopen.2026.34372,
title = {Diagnosis Through Whole Genome Sequencing and Care Utilization in Children With Severe Illness.},
author = {Dias JML and More RP and Butler D and Brown J and French CE and Dolling H and Raymond FL and Rowitch DH and Aiken CE},
year = {2026},
journal = {JAMA network open},
doi = {10.1001/jamanetworkopen.2026.34372},
url = {https://doi.org/10.1001/jamanetworkopen.2026.34372}
}RIS
TY - JOUR TI - Diagnosis Through Whole Genome Sequencing and Care Utilization in Children With Severe Illness. AU - Dias JML AU - More RP AU - Butler D AU - Brown J AU - French CE AU - Dolling H AU - Raymond FL AU - Rowitch DH AU - Aiken CE PY - 2026 JO - JAMA network open DO - 10.1001/jamanetworkopen.2026.34372 UR - https://doi.org/10.1001/jamanetworkopen.2026.34372 ER -
APA
JML, D., RP, M., D, B., J, B., CE, F., H, D., FL, R., DH, R., & CE, A. (2026). Diagnosis Through Whole Genome Sequencing and Care Utilization in Children With Severe Illness.. JAMA network open. https://doi.org/10.1001/jamanetworkopen.2026.34372
Source records
- pubmed · retrieved 2026-09-25T18:45:16.866Z