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Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.
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Genetic transmission of Alzheimer's disease among families in a Dutch population based study.
Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.
Inversions in the factor VIII gene: improvement of carrier detection and prenatal diagnosis in Dutch haemophilia A families.
Genetic heterogeneity of Usher syndrome type II in a Dutch population.
Histocompatibility antigens in multiple sclerosis patients participating in a multicentre trial of azathioprine. British & Dutch Multiple Sclerosis Azathioprine Trial Group.
Autosomal dominant congenital Horner's syndrome in a Dutch family.
TIA, RIND, minor stroke: a continuum, or different subgroups? Dutch TIA Study Group.
Hereditary cerebral haemorrhage with amyloidosis, Dutch type (HCHWA-D): clinicopathological studies.
Recurrent stroke after transient ischaemic attack or minor ischaemic stroke: does the distinction between small and large vessel disease remain true to type? Dutch TIA Trial Study...