Ellien van der Kooij-Meijs

Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in dutch families

Arie van Haeringen, Wilma Bergman, Marcel Nelen et al. · Genomics · 1989 · 81 citations

Down Syndrome, Dutch Families, Mendelian Disorder +10

Genetic heterogeneity in familial dysbetalipoproteinemia. The E2(lys146—-gln) variant results in a dominant mode of inheritance.

M. Smit, Peter de Knijff, Ellien van der Kooij-Meijs et al. · Journal of Lipid Research · 1990 · 73 citations · Full text

Apolipoprotein gene cluster on chromosome 19

M. Smit, Ellien van der Kooij-Meijs, Rune R. Frants et al. · Human Genetics · 1988 · 64 citations

Apolipoprotein Gene Cluster, Cytogenetics, Genetic Disorder +7

A common restriction fragment length polymorphism of the human apolipoprotein E gene and its relationship to type III hyperlipidaemia

E.C. Klasen, Philippa J. Talmud, Louis M. Havekes et al. · Human Genetics · 1987 · 31 citations

Lipid Disorder, Allelic Variant, Genetics +9

Exact localization of the familial dysretalipoproteinemia associated HPAI restriction site in the promoter region of the APOC1 gene

M. Smit, Ellien van der Kooij-Meijs, Lambertus P. Woudt et al. · Biochemical and Biophysical Research Communications · 1988 · 27 citations

Transcriptional Regulation, Allelic Variant, Genetic Disorder +12