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Browsing by Author Donk, K.P. van der
Showing results 1 to 4 of 4
| Full Text | Issue Date | Title | Author(s) | | 2009 | Clinical and molecular evaluation of probands and family members with familial exudative vitreoretinopathy. | Boonstra, F.N.; Nouhuys, C.E. van; Schuil, J.; Wijs, I.J. de; Donk, K.P. van der, et al |
| 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 |
| 2006 | CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene. | Jongmans, M.C.J.; Admiraal, R.J.C.; Donk, K.P. van der; Vissers, L.E.L.M.; Baas, A., et al |
| 2005 | Hearing impairment in Dutch patients with connexin 26 (GJB2) and connexin 30 (GJB6) mutations. | Santos, R.L.; Aulchenko, Y.S.; Huygen, P.L.M.; Donk, K.P. van der; Wijs, I.J. de, et al |
Showing results 1 to 4 of 4
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