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European Journal of Medical Genetics|December 29, 2010
15q11.2 microdeletion - seven new patients with delayed development and/or behavioural problemsC von der Lippe, C Rustad, K Heimdal, et al.Clinical Genetics|May 14, 2015
Mutation analysis in Norwegian families with hereditary hemorrhagic telangiectasia: founder mutations in ACVRL1K Heimdal, B Dalhus, O K Rødningen, et al.Scandinavian Journal of Clinical and Laboratory Investigation|February 1, 1996
Application of long polymerase chain reaction in the study of the LDL receptor geneO K Rødningen, T P LerenComputer Methods and Programs in Biomedicine|February 5, 2000
The genetic algorithm applied to haplotype data at the LDL receptor locusO Braaten, O K Rødningen, I Nordal, et al.Scandinavian Journal of Clinical and Laboratory Investigation|December 1, 1994
Familial hypercholesterolaemia caused by a non-sense mutation in codon 329 of the LDL receptor geneK Solberg, O K Rødningen, S Tonstad, et al.The Journal of Cell Biology|June 1, 1971
Nuclear-cytoplasmic relations in the mitosis of sea urchin eggs. 3. Gamma-ray--induced damage to whole eggs and nucleate and anucleate half-eggsR C Rustad, S Yuyama, L C RustadHuman Genetics|August 1, 1995
Two novel point mutations in the EGF precursor homology domain of the LDL receptor gene causing familial hypercholesterolemiaT P Leren, K Solberg, O K Rødningen, et al.Biotechniques|April 1, 1993
Screening for point mutations by semi-automated DNA sequencing using sequenase and magnetic beadsT P Leren, O K Rødningen, O Røsby, et al.Human Mutation|July 22, 1998
Effects of a 9.6-kb deletion of the LDL receptor gene (FH Helsinki) on structure and levels of mRNAO K Rødningen, S Tonstad, L Ose, et al.Atherosclerosis|December 1, 1994
Two founder mutations in the LDL receptor gene in Norwegian familial hypercholesterolemia subjectsT P Leren, K Solberg, O K Rødningen, et al.Pageof 9