1.
A small interstitial deletion in the GPC3 gene causes Simpson-Golabi-Behmel syndrome in a Dutch-Canadian family
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree
Mortality in patients with epilepsy: 40 years of follow up in a Dutch cohort study
Thrombolysis for acute stroke with special emphasis on the very old: experience from a single Dutch centre
Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology