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Browsing by Author Laar, I. van de
Showing results 1 to 3 of 3
| Full Text | Issue Date | Title | Author(s) | | 2008 | Familial 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 |
| 2007 | Limb 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 |
| 2005 | Familial gigantism caused by an NSD1 mutation. | Haelst, M.M. van; Hoogeboom, J.J.; Baujat, G.; Bruggenwirth, H.T.; Laar, I. van de, et al |
Showing results 1 to 3 of 3
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