J. Begeer

发表

Recurrent mutation 4882delTT in the GAP‐related domain of the tuberous sclerosis TSC2 gene

S. Verhoef, D. Lindhout, S. Jóźwiak, 1998, Human mutation.

H. Scheffer, C. Buys, G. van Ommen, 1994, Journal of medical genetics.

The prognostic value of serial EEG recordings following acute neonatal asphyxia in full-term infants.

N. Maurits, J. Fock, E. Zeinstra, 2001, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

CSF choline levels in neurologically disturbed children

A. Teelken, F. Flentge, J. Begeer, 1989, Acta neurologica Scandinavica.

Analysis of different treatment modalities of tethered cord syndrome

E. Hoving, J. Begeer, W. V. D. van der Meulen, 2002, Child's Nervous System.

Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation

W. Ruitenbeek, H. Bentlage, J. Begeer, 1994, Journal of the Neurological Sciences.

Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration.

J. J. Shepherd, D. Sillence, L. Mestroni, 1994, Journal of medical genetics.