1. aciduria and, 3-methylcrotonylglycinuria: a new inborn error of metabolism;Eldjarn, L.; Jellum, E.; Stokke, O.; Pande, H.; Waaler, P.E.;Lancet,1970
2. Gas-chromatographic diagnosis of intermittent maple syrup urine disease (branchchain ketoaciduria);Gompertz, D.; Draffan, G.H.;Clinica Chimica Acta,1972
3. Identification of tiglylglycine in the urine of a child with,3-methylcrotonylglycinuria;Gompes-tz, D.; Draffan, G.H.;Clinica Chimica Acta,1972
4. Gompertz, D., Draffan, G. H., Watts, J. L., and Hull, D. (1971).
5. 3-methylcrotonyl-CoA carboxylase deficiency: a new metabolic error in leucine degradation;Stokke, O.; Eldjarn, L.; Jellum, E.; Pande, H.; Waaler, P.E.;Pediatrics,1972