Aldur W. Eriksson

The Cowden syndrome: a clinical and genetic study in 21 patients

Th. M. Starink, J.P.W. van der Veen, F. Arwert et al. · Clinical Genetics · 1986 · 550 citations

Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia

Hans Joenje, Fré Arwert, Aldur W. Eriksson et al. · Nature · 1981 · 276 citations

Biology, Chromatin, Cell Division +9

Molecular heterogeneity of steroid sulfatase deficiency: A multicenter study on 57 unrelated patients, at DNA and protein levels

Andrea Ballabio, Rosalba Carrozzo, Giancarlo Parenti et al. · Genomics · 1989 · 102 citations

Unrelated Patients, Biochemistry, Inherited Metabolic Disease +6

The human α-amylase multigene family consists of haplotypes with variable numbers of genes

Peter C. Groot, Maria J. Bleeker, Jan C. Pronk et al. · Genomics · 1989 · 93 citations

Genetic Analysis, Allelic Variant, Haplotype Determination +7

Historical epidemiology of smallpox in Åland, Finland: 1751–1890

James H. Mielke, Lynn B. Jorde, P. Gene Trapp et al. · Demography · 1984 · 85 citations · Full text