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Lancet (London, England)|December 15, 1979
Dihydropteridine reductase deficiency diagnosis by assays on peripheral blood-cellsF A Firgaira, R G Cotton, D M DanksAmerican Journal of Human Genetics|October 1, 1988
Application of DNA-DNA hybridization of dual labeled probes to the detection of trisomy 21, monosomy 21, and sex determinationH H Dahl, K H Choo, D M DanksClinica Chimica Acta; International Journal of Clinical Chemistry|May 2, 1977
A new sulfur amino acid, named hawkinsin, identified in a baby with transient tyrosinemia and her motherA Niederwieser, A Matasovic, P Tippett, et al.American Journal of Medical Genetics|October 1, 1984
Mental retardation, unusual face, and intrauterine growth retardation: a new recessive syndrome?D B Pitt, J G Rogers, D M DanksThe Biochemical Journal|July 1, 1981
Isolation and characterization of dihydropteridine reductase from human liverF A Firgaira, R G Cotton, D M DanksThe Medical Journal of Australia|November 2, 1987
Mild Sanfilippo syndrome: a further cause of hyperactivity and behavioural disturbanceJ E Wraith, D M Danks, J G RogersBiological Trace Element Research|December 1, 1989
Zinc transport by fibroblasts from patients with acrodermatitis enteropathicaM L Ackland, D M Danks, H J McArdleHuman Genetics|January 1, 1985
Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: plasma changes and skin fibroblast phytanic acid oxidaseA Poulos, P Sharp, A J Fellenberg, et al.American Journal of Human Genetics|September 1, 1983
Mutations at more than one locus may be involved in cystic fibrosis--evidence based on first-cousin data and direct counting of casesD M Danks, J Allan, P D Phelan, et al.Journal of Inherited Metabolic Disease|January 1, 1995
Trimethylaminuria, fish odour syndrome: a new method of detection and response to treatment with metronidazoleE Treacy, D Johnson, J J Pitt, et al.Pageof 17