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P T Clayton

Showing results (1-10 of 101) with videos related to

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Archives of Disease in Childhood|May 14, 1998
Disorders of cholesterol biosynthesisP T Clayton
Journal of Inherited Metabolic Disease|August 2, 2003
Diagnosis of inherited disorders of liver metabolismP T Clayton
The Journal of Pediatrics|November 1, 1994
Delta 4-3-oxosteroid 5 beta-reductase deficiency and neonatal hemochromatosisP T Clayton
Journal of Inherited Metabolic Disease|June 19, 2001
Applications of mass spectrometry in the study of inborn errors of metabolismP T Clayton
Biochemical Society Transactions|May 18, 2001
Clinical consequences of defects in peroxisomal beta-oxidationP T Clayton
Journal of Inherited Metabolic Disease|January 1, 1991
Inborn errors of bile acid metabolismP T Clayton
American Journal of Medical Genetics|April 10, 1995
Concerning "Agamanolis disease"P T Clayton, N Mian
Journal 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 Grunewald
Clinical Chemistry|December 1, 1992
Aromatic L-amino acid decarboxylase deficiency: diagnostic methodologyK Hyland, P T Clayton
Journal of Inherited Metabolic Disease|January 1, 1990
Aromatic amino acid decarboxylase deficiency in twinsK Hyland, P T Clayton
Pageof 11

Showing results (1-10 of 101) with videos related to

Sort By:
Pageof 11
Archives of Disease in Childhood|May 14, 1998
Disorders of cholesterol biosynthesisP T Clayton
Journal of Inherited Metabolic Disease|August 2, 2003
Diagnosis of inherited disorders of liver metabolismP T Clayton
The Journal of Pediatrics|November 1, 1994
Delta 4-3-oxosteroid 5 beta-reductase deficiency and neonatal hemochromatosisP T Clayton
Journal of Inherited Metabolic Disease|June 19, 2001
Applications of mass spectrometry in the study of inborn errors of metabolismP T Clayton
Biochemical Society Transactions|May 18, 2001
Clinical consequences of defects in peroxisomal beta-oxidationP T Clayton
Journal of Inherited Metabolic Disease|January 1, 1991
Inborn errors of bile acid metabolismP T Clayton
American Journal of Medical Genetics|April 10, 1995
Concerning "Agamanolis disease"P T Clayton, N Mian
Journal 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 Grunewald
Clinical Chemistry|December 1, 1992
Aromatic L-amino acid decarboxylase deficiency: diagnostic methodologyK Hyland, P T Clayton
Journal of Inherited Metabolic Disease|January 1, 1990
Aromatic amino acid decarboxylase deficiency in twinsK Hyland, P T Clayton
Pageof 11