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Browsing by Author Laar, I. van de

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Full TextIssue DateTitleAuthor(s)
2008Familial CHARGE syndrome and the CHD7 gene: a recurrent missense mutation, intrafamilial recurrence and variability.Jongmans, M.C.J.; Hoefsloot, L.H.; Donk, K.P. van der; Admiraal, R.J.; Magee, A., et al
2007Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype.Laar, I. van de; Dooijes, D.; Hoefsloot, L.H.; Simon, M.; Hoogeboom, J., et al
2005Familial gigantism caused by an NSD1 mutation.Haelst, M.M. van; Hoogeboom, J.J.; Baujat, G.; Bruggenwirth, H.T.; Laar, I. van de, et al
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