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Journal of Inherited Metabolic Disease|January 1, 1989
Use of placental enzyme analysis in assessment of the newborn at risk for non-ketotic hyperglycinaemia (NKH)J R Toone, D A ApplegarthJournal of Inherited Metabolic Disease|July 27, 2004
Glycine encephalopathy (nonketotic hyperglycinaemia) : review and updateD A Applegarth, J R TooneMolecular Genetics and Metabolism|October 11, 2001
Nonketotic hyperglycinemia (glycine encephalopathy): laboratory diagnosisD A Applegarth, J R ToonePediatrics|January 5, 2000
Incidence of inborn errors of metabolism in British Columbia, 1969-1996D A Applegarth, J R Toone, R B LowryJournal of Inherited Metabolic Disease|January 1, 1992
Prenatal diagnosis of non-ketotic hyperglycinaemiaJ R Toone, D A Applegarth, H L LevyPediatric Clinics of North America|February 1, 1989
Laboratory detection of metabolic diseaseD A Applegarth, J E Dimmick, J R ToonePediatric Pathology|January 1, 1983
Laboratory diagnosis of inborn errors of metabolism in childrenD A Applegarth, J R Toone, P M MacLeodPrenatal Diagnosis|November 1, 1986
Prenatal diagnosis of infantile GM 2 gangliosidosis type II (Sandhoff disease) by detection of N-acetylglucosaminyl-oligosaccharides in amniotic fluid with high-performance liquid chromatographyT G Warner, M W Turner, J R Toone, et al.Clinical Biochemistry|January 7, 1999
A protocol for detection of mitochondrial DNA deletions: characterization of a novel deletionM B Coulter-Mackie, D A Applegarth, J R Toone, et al.Pageof 3