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Browsing by Author Verhoeven, K.

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Showing results 1 to 5 of 5
Full TextIssue DateTitleAuthor(s)
2009Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy.Claeys, K.G.; Zuchner, S.; Kennerson, M.; Berciano, J.; Garcia, A., et al
1997Vroeg manifesterend erfelijk gehoorverlies met late neurologische klachten exclusief overervend langs de moederlijke lijn.Ensink, R.J.H.; Marres, H.A.M.; Huygen, P.L.M.; Verhoeven, K.; Padberg, G.W.A.M., et al
1997Vroeg manifesterend erfelijk gehoorverlies met late neurologische klachten exclusief overervend langs de moederlijke lijn.Marres, H.A.M.; Huygen, P.L.M.; Verhoeven, K.; Padberg, G.W.A.M.; Cremers, C.W.R.J.
1997Early onset inherited hearing loss and late onset neurological complaints with maternal inheritanceEnsink, R.J.H.; Marres, H.A.M.; Huygen, P.L.M.; Verhoeven, K.; Padberg, G.W.A.M., et al
1996Early onset maternal inherited hearing loss with late onset neurological symptoms present in a three generation Dutch family.Ensink, R.J.H.; Marres, H.A.M.; Cremers, C.W.R.J.; Huygen, P.L.M.; Verhoeven, K., et al
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