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European Journal of Pediatrics|August 1, 1993
Molybdenum cofactor deficiency in two siblings: diagnostic difficultiesL K Hansen, K Wulff, C Dorche, et al.
Prenatal Diagnosis|May 18, 1999
Molybdenum cofactor deficiency: first prenatal genetic analysisJ Reiss, E Christensen, C Dorche
Ugeskrift for Laeger|June 21, 1993
[Trichothiodystrophy. Hair examination as a diagnostic tool]L K Hansen, K Wulff, F Brandrup
Ugeskrift for Laeger|April 10, 1995
[Ataxia telangiectasia]L K Hansen, K Wulff, N J Seersholm
Human Genetics|January 28, 1999
Genomic structure and mutational spectrum of the bicistronic MOCS1 gene defective in molybdenum cofactor deficiency type AJ Reiss, E Christensen, G Kurlemann, et al.
Ugeskrift for Laeger|September 15, 2000
[Zellweger syndrome--a peroxisomal disease]L K Hansen, E Christensen, B B Jacobsen
Archives of Biochemistry and Biophysics|November 1, 1990
Studies on the interaction of a thiol-dependent hydrogen peroxide scavenging enzyme and phenylalanine hydroxylaseS Milstien, C Dorche, S Kaufman
Arzneimittel-Forschung|January 1, 1986
Nucleic acids as analytes in laboratory diagnosisK Wulff
Acta Orthopaedica Scandinavica|December 1, 1982
Epidemiology and treatment of distal femoral fractures in adultsL Kolmert, K Wulff
Acta Anaesthesiologica Scandinavica|June 1, 1979
Regional lung function following hip arthroplasty and preoperative normovolemic hemodilutionB Rosberg, K Wulff
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