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Human Genetics|February 1, 1992
Transferrin subtypes in 51 Danish patients with hereditary haemochromatosis and in 847 normal subjectsN Milman, H Eiberg, M Thymann, et al.American Journal of Community Psychology|December 1, 1976
Perspectives of clinical students on training in community mental health and community psychologyE Zolik, W Sirbu, D HopkinsonActa Anaesthesiologica Scandinavica|August 1, 1984
Controlled ventilation using the Lack circuit with an injector deviceN D Hopkinson, M J HarrisonThe Journal of Biological Chemistry|November 5, 1991
Human red cell acid phosphatase (ACP1). The amino acid sequence of the two isozymes Bf and Bs encoded by the ACP1*B alleleJ Dissing, A H Johnsen, G F SensabaughAnnals of Human Genetics|March 30, 2000
Rapid and simple determination of hereditary haemochromatosis mutations by multiplex PCR-SSCP: detection of a new polymorphic mutationK Simonsen, J Dissing, L Rudbeck, et al.Biochemical and Biophysical Research Communications|October 15, 1993
Exon structure at the human ACP1 locus supports alternative splicing model for f and s isozyme generationK D Lazaruk, J Dissing, G F SensabaughJournal of Clinical Pathology|January 1, 1992
Classical complement activation induced by pregnancy: implications for management of connective tissue diseasesN D Hopkinson, R J PowellToxicology in Vitro : an International Journal Published in Association with BIBRA|August 25, 2010
In vitro cytotoxicity testing: Biological and statistical significanceF A Barile, S Arjun, D HopkinsonAnnals of Human Genetics|March 14, 2001
Human 18 kDa phosphotyrosine protein phosphatase (ACP1) polymorphism: studies of rare variants provide evidence that substitutions within or near alternatively spliced exons affect splicing resultL Rudbeck, J Dissing, K D Lazaruk, et al.Human Genetics|January 1, 1985
Unusual sialilation of three different rare genetic variants of serum DBP: Gc1A17, Gc1A16, and Gc1A11M Thymann, B Hoste, W Scheffrahn, et al.Pageof 7