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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., van Dijk, F. S., de Reuver, R., de Kruiff, C., Pondaag, W. & Hennekam, R. C., 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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Question 2 Does combined oral dexamethasone and epinephrine inhalation help infants with bronchiolitis to recover faster?
van Dellen, Q. M., Kreier, F., de Kruiff, C. C., Boluyt, N. & Fijnvandraat, K., 2011, In: Archives of disease in childhood. 96, 6, p. 606-608Research output: Contribution to journal › Editorial › Academic › peer-review
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