Many newborns in level IV NICUs are eligible for rapid DNA sequencing
Author:
Affiliation:
1. Children's Hospital & Medical Center and Department of PediatricsUniversity of Nebraska Medical Center Omaha Nebraska
2. Munroe‐Meyer Institute for Genetics and RehabilitationUniversity of Nebraska Medical Center Omaha Nebraska
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61011
Reference9 articles.
1. A rapid gene sequencing panel strategy to facilitate precision neonatal medicine
2. Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing
3. Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit
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5. A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases
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3. Rapid exome sequencing as a first-tier test in neonates with suspected genetic disorder: results of a prospective multicenter clinical utility study in the Netherlands;European Journal of Pediatrics;2023-03-31
4. Ethical Considerations for Equitable Access to Genomic Sequencing for Critically Ill Neonates in the United States;International Journal of Neonatal Screening;2022-03-21
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