A clinical utility study of diagnosing genetic disorders in newborns admitted to the Neonatal Intensive Care Unit
A. C. Deden,L. E. L. M. Vissers,R. A. C. M. Olde Keizer,G. W. J. Frederix,P. Andriessen,K. A. Bergman,R. A. van Lingen,L. S. de Vries,K. D. Lichtenbelt,W. S. Kerstjens-Frederikse, I. P. C. Krapels,J. S. Klein Wassink-Ruiter,K. Neveling,M. Nelen, S. Castelein, M. del Rosario, S. van den Heuvel,C. Gilissen,E. Kamsteeg,R. Pfundt,T. Rinne,H. G. Yntema,R. J. Sinke,W. P. de Boode,W. A. G. Zelst-Stams EUROPEAN JOURNAL OF HUMAN GENETICS(2019)
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genetic disorders,newborns,intensive care,intensive care unit
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