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.

MLA

Olde 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, June 2023, pp. 2683–92. EBSCOhost, https://doi.org/10.1007/s00431-023-04909-1.

APA

Olde Keizer, R. A. C. M., Marouane, A., Kerstjens-Frederikse, W. S., Deden, A. C., Lichtenbelt, K. D., Jonckers, T., Vervoorn, M., Vreeburg, M., Henneman, L., de Vries, L. S., Sinke, R. J., Pfundt, R., Stevens, S. J. C., Andriessen, P., van Lingen, R. A., Nelen, M., Scheffer, H., Stemkens, D., Oosterwijk, C., & 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), 2683–2692. https://doi.org/10.1007/s00431-023-04909-1

Chicago

Olde Keizer, Richelle A. C. M., Abderrahim Marouane, Wilhelmina S. Kerstjens-Frederikse, A. Chantal Deden, Klaske D. Lichtenbelt, Tinneke Jonckers, Marieke Vervoorn, et al. 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): 2683–92. doi:10.1007/s00431-023-04909-1.