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The Biochemical Journal|February 15, 1982
Copper metabolism in mottled mouse mutants. The effect of copper therapy on lysyl oxidase activity in brindled (Mobr) miceP M Royce, J Camakaris, J R Mann, et al.Journal of Medical Genetics|January 1, 1988
The use of restriction fragment length polymorphisms in prenatal diagnosis of dihydropteridine reductase deficiencyH H Dahl, S Wake, R G Cotton, et al.Archives of Disease in Childhood|May 1, 1985
Long term prognosis for babies with neonatal liver diseaseJ Deutsch, A L Smith, D M Danks, et al.Journal of Inherited Metabolic Disease|January 1, 1981
Two-dimensional polyacrylamide gel analysis of fibroblast polypeptides: discussion of its relevance for inherited diseasesK H Choo, R G Cotton, D M Danks, et al.Archives of Disease in Childhood|May 1, 1977
Prognosis of babies with neonatal hepatitisD M Danks, P E Campbell, A L Smith, et al.The Journal of Pediatrics|December 1, 1976
Chondrodysplasia punctata-23 cases of a mild and relatively common varietyL J Sheffield, D M Danks, V Mayne, et al.Journal of Inherited Metabolic Disease|January 1, 1984
Malonyl coenzyme A decarboxylase deficiencyG K Brown, R D Scholem, A Bankier, et al.Journal of Medical Genetics|April 1, 1979
Achondroplasia and hypochondroplasia. Comments on frequency, mutation rate, and radiological features in skull and spineF Oberklaid, D M Danks, F Jensen, et al.The Biochemical Journal|June 15, 1979
Copper metabolism in mottled mouse mutants: copper therapy of brindled (Mobr) miceJ R Mann, J Camakaris, D M Danks, et al.Journal of Inherited Metabolic Disease|January 1, 1983
Mutations in humans and animals which affect copper metabolismJ Camakaris, M Phillips, D M Danks, et al.Pageof 19