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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.Archives of Pathology & Laboratory Medicine|January 1, 1983
Analyzing the factors contributing to rising laboratory costsJ Tydeman, J I Morrison, P A Cassidy, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|May 30, 1986
Fluorometric determination of nanogram quantities of protein in small samples: application to calcium-transport adenosine triphosphataseM A Bridges, K M McErlane, E Kwong, et al.Journal of Clinical Engineering|September 8, 1983
Clinical chemistry equipment: a computerized system for cost evaluationJ I Morrison, J Tydeman, P A Cassidy, et al.Molecular Genetics and Metabolism|June 30, 2000
Biochemical and molecular investigations of patients with nonketotic hyperglycinemiaJ R Toone, D A Applegarth, M B Coulter-Mackie, et al.Human Mutation|January 4, 2001
Identification of the first reported splice site mutation (IVS7-1G-->A) in the aminomethyltransferase (T-protein) gene (AMT) of the glycine cleavage complex in 3 unrelated families with nonketotic hyperglycinemiaJ R Toone, D A Applegarth, M B Coulter-Mackie, et al.Molecular Genetics and Metabolism|April 5, 2001
Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N145I): a strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH)J R Toone, D A Applegarth, M B Coulter-Mackie, et al.Pediatric Research|March 1, 1975
Metabolic studies of a family with massive formiminoglutamic aciduriaT L Perry, D A Applegarth, M E Evans, et al.Journal of Child Neurology|November 26, 1999
Atypical nonketotic hyperglycinemia with normal cerebrospinal fluid to plasma glycine ratioA H Jackson, D A Applegarth, J R Toone, et al.Pageof 14