1. Roe, C.R. & Coates, P. (1995) In The metabolic and molecular bases of inherited disease. 1501–1534 Mitochondrial fatty acid oxidation disorders (Scriver, C., Beaudet, A.L., Sly, W.S. & Valle, D. eds.) 7th ed. MGraw-Hill, New York.
2. Iafolla, A.K., Thompson, R.J. & Roe, C.R. (1994) J Pediatr. 124, 409–415 Medium chain acyl-CoA-dehydrogenase deficiency: clinical course in 120 affected children.
3. Rinaldo, P. (1994) In Liver disease in Children. 295–308 Laboratory diagnosis of inborn errors of metabolism. (Suchy, F.J. ed.) Mosby, St. Louis.
4. Stanley, C.A. (1995) In Inborn Metabolic Diseases. Diagnosis and Treatment. 133–146 Disorders of fatty acid oxidation. (Fernandes, J., Saudubray, J.M. & Van den Berghe G. eds). 2nd, Ed. Springer-Verlag, Berlin.
5. Van Hove, J.L.K., Zhang, W., Kahler, S.G., Roe, C.R., Chen, Y.T., Terada, N., Chase, D., Iafolla, K., Ding, J.H. & Millington, D. (1993) Am J Hum Genet. 52, 958–66 Medium chain Acyl-CoA dehydrogenase (MCAD) deficiency: Diagnosis by acylcarnitine in blood.