Olde Keizer, R. A. C. M., Marouane, A., Kerstjens-Frederikse, W. S., Deden, A. C., Lichtenbelt, K. D., Jonckers, T., . . . van Amstel, H. K. P. (2023). 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, 182(6), 2683. https://doi.org/10.1007/s00431-023-04909-1
Chicago Style (17th ed.) CitationOlde Keizer, Richelle A. C. M., et al. "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 182, no. 6 (2023): 2683. https://doi.org/10.1007/s00431-023-04909-1.
MLA (9th ed.) CitationOlde Keizer, Richelle A. C. M., et al. "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, vol. 182, no. 6, 2023, p. 2683, https://doi.org/10.1007/s00431-023-04909-1.