1.

Genome-wide screen in obese pedigrees with type 2 diabetes mellitus from a defined Dutch population

1.

Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family

1.

Rapid N-acetyltransferase 2 imputed phenotype and smoking may increase risk of colorectal cancer in women (Netherlands)

1.

Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.

2.

Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.

3.

Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.

1.

A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q

1.

Linkage disequilibrium in young genetically isolated Dutch population

2.

Linkage disequilibrium in young genetically isolated Dutch population

3.

Linkage disequilibrium in young genetically isolated Dutch population

1.

A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the Netherlands

1.

A genome-wide search for genes involved in type 2 diabetes in a recently genetically isolated population from the Netherlands

1.

Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group

1.

17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations