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Anticipating the future of the child and family in pediatric palliative care: a qualitative study into the perspectives of parents and healthcare professionals
Verberne, L. M., Fahner, J. C., Sondaal, S. F. V., Schouten–van Meeteren, A. Y. N., de Kruiff, C. C., van Delden, J. J. M. & Kars, M. C., Mar 2021, In: European journal of pediatrics. 180, 3, p. 949-957 9 p.Research output: Contribution to journal › Article* › Academic › peer-review
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A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability
Cobben, J. M., Weiss, M. M., van Dijk, F. S., de Reuver, R., de Kruiff, C., Pondaag, W., Hennekam, R. C. & Yntema, H. G., 2014, In: European journal of medical genetics. 57, 11-12, p. 636-638Research output: Contribution to journal › Article* › Academic › peer-review
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Milde laryngitis subglottica: Wel of niet medicamenteus behandelen?
de Kruiff, C. C. & Boluyt, N., 2011, In: Praktische pediatrie. 2011, juni, p. 55Research output: Contribution to journal › Article* › Professional
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