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Journal of Inherited Metabolic Disease|January 1, 1980
Abnormal copper metabolism in cultured fibroblasts from patients with Wilson's diseaseJ Camakaris, L Ackland, D M DanksBiomedical Mass Spectrometry|March 1, 1981
Two new sulphur-containing amino acids in manR J Truscott, D Malegan, E McCairns, et al.The Biochemical Journal|February 15, 1980
Copper metabolism in mottled mouse mutants. Defective placental transfer of 64Cu to foetal brindled (Mobr) miceJ R Mann, J Camakaris, D M DanksThe Biochemical Journal|June 15, 1979
Copper metabolism in mottled mouse mutants: distribution of 64Cu in brindled (Mobr) miceJ R Mann, J Camakaris, D M DanksEuropean Journal of Pediatrics|April 1, 1993
Non-specific elevation of immunoreactive trypsinogen in sick infantsD Ravine, R I Francis, D M DanksThe Biochemical Journal|November 15, 1980
Reduced lysyl oxidase activity in skin fibroblasts from patients with Menkes' syndromeP M Royce, J Camakaris, D M DanksSomatic Cell and Molecular Genetics|July 1, 1984
Observations on the Menkes' and brindled mouse phenotypes in cell hybridsR M Brown, J Camakaris, D M DanksJournal of Medical Genetics|April 1, 1979
Genetic heterogeneity in osteogenesis imperfectaD O Sillence, A Senn, D M DanksThe Biochemical Journal|June 15, 1979
Copper metabolism in mottled mouse mutants: copper concentrations in tissues during developmentJ Camakaris, J R Mann, D M DanksPediatrics|October 1, 1982
beta-hydroxyisobutyryl coenzyme A deacylase deficiency: a defect in valine metabolism associated with physical malformationsG K Brown, S M Hunt, R Scholem, et al.Pageof 19