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Editorial
. 2024 Aug 1;25(8):761-764.
doi: 10.1097/PCC.0000000000003548. Epub 2024 Aug 5.

Applying Genomic Medicine to Critically Ill Children, Science and Fiction

Affiliations
Editorial

Applying Genomic Medicine to Critically Ill Children, Science and Fiction

Ricardo G Branco et al. Pediatr Crit Care Med. .
No abstract available

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Conflict of interest statement

The authors have disclosed that they do not have any potential conflicts of interest.

References

    1. Collins FS, McKusick VA: Implications of the Human Genome Project for medical science. JAMA. 2001; 285:540–544
    1. Krantz ID, Medne L, Weatherly JM, et al.; NICUSeq Study Group: Effect of whole-genome sequencing on the clinical management of acutely ill infants with suspected genetic disease: A randomized clinical trial [published correction appears in JAMA Pediatr . 2021 December 1;175(12):1295]. JAMA Pediatr. 2021; 175:1218–1226
    1. Rodriguez KM, Vaught J, Salz L, et al.: Rapid Whole-Genome Sequencing and Clinical Management in the PICU: A Multi-Center Cohort, 2016–2023. Pediatr Crit Care Med. 2024; 25:699–709
    1. Wu ET, Hwu WL, Chien YH, et al.: Critical trio exome benefits in-time decision-making for pediatric patients with severe illnesses. Pediatr Crit Care Med. 2019; 20:1021–1026
    1. Lunke S, Eggers S, Wilson M, et al.; Australian Genomics Health Alliance Acute Care Flagship: Feasibility of ultra-rapid exome sequencing in critically ill infants and children with suspected monogenic conditions in the Australian public health care system. JAMA. 2020; 323:2503–2511

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