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Journal of Inherited Metabolic Disease|August 2, 2003
Diagnosis of inherited disorders of liver metabolismP T ClaytonJournal of Inherited Metabolic Disease|June 19, 2001
Applications of mass spectrometry in the study of inborn errors of metabolismP T ClaytonBiochemical Society Transactions|May 18, 2001
Clinical consequences of defects in peroxisomal beta-oxidationP T ClaytonJournal of Inherited Metabolic Disease|January 1, 1991
Inborn errors of bile acid metabolismP T ClaytonJournal of Inherited Metabolic Disease|March 10, 2009
Comprehensive description of the phenotype of the first case of congenital disorder of glycosylation due to RFT1 deficiency (CDG In)P T Clayton, S GrunewaldClinical Chemistry|December 1, 1992
Aromatic L-amino acid decarboxylase deficiency: diagnostic methodologyK Hyland, P T ClaytonJournal of Medical Genetics|July 1, 1988
Dysmorphic syndromes with demonstrable biochemical abnormalitiesP T Clayton, E ThompsonAdvances in Internal Medicine|January 1, 1990
Diagnosis and management of liver disease in pregnancyM L WilkinsonJournal of Inherited Metabolic Disease|January 1, 1994
Phytanic acid alpha-oxidase deficiency (Refsum disease) presenting in infancyM A Herbert, P T ClaytonPageof 13