Steen K�lvraa

Oligonucleotide-priming methods for the chromosome-specific labelling of alpha satellite DNA in situ

J�rn E. Koch, Steen K�lvraa, Kirsten Bruun Petersen et al. · Chromosoma · 1989 · 294 citations

Biology, Chromatin, Chromosome-specific Labelling +13

Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli

Niels Gregersen, Brage Storstein Andresen, Peter Bross et al. · Human Genetics · 1991 · 72 citations · Full text

E. Coli, Cellular Enzymology, Biochemistry +8

Simultaneous detection of centromere-specific probes and chromosome painting libraries by a combination of primedin situ labelling and chromosome painting (PRINS-painting)

J. Hindkj�r, C A Brandt, Jørn Koch et al. · Chromosome Research · 1995 · 25 citations

Chromatin, Genetic Testing, Chromosome Dynamics +11

Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12

Steen K�lvraa, TorbenA. Kruse, P. K. A. Jensen et al. · Human Genetics · 1986 · 21 citations

Close Linkage, Allelic Variant, Genetic Disorder +8

The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene

Steen K�lvraa, Niels Gregersen, Alexandra I. F. Blakemore et al. · Human Genetics · 1991 · 21 citations

Allelic Variant, Particular Haplotype, Common Mutation +8