Perspectives of United States neonatologists on genetic testing practices
Author:
Funder
Eunice Kennedy Shriver National Institute of Child Health and Human Development
National Institutes of Health
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference19 articles.
1. Use of exome sequencing for infants in intensive care units: ascertainment of severe single-gene disorders and effect on medical management;Meng;JAMA Pediatr,2017
2. Making a genetic diagnosis in a level IV neonatal intensive care unit population: who, when, how, and at what cost?;Swaggart;J Pediatr,2019
3. Infant mortality: the contribution of genetic disorders;Wojcik;J Perinatol,2019
4. Benchmarking outcomes in the neonatal intensive care unit: cytogenetic and molecular diagnostic rates in a retrospective cohort;Malam;Am J Med Genet A,2017
5. Prospective, phenotype-driven selection of critically ill neonates for rapid exome sequencing is associated with high diagnostic yield;Gubbels;Genet Med,2020
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5. Ethical and Legal Issues Surrounding Genetic Testing in the NICU;NeoReviews;2024-03-01
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