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Journal of Medical Genetics
|
July 1, 1988
Dysmorphic syndromes with demonstrable biochemical abnormalities
P T Clayton, E Thompson
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 19, 1980
A simplified gas-liquid chromatographic methods for the estimation of non-sulphated plasma bile acids
P T Clayton, D P Muller
Journal of Inherited Metabolic Disease
|
January 1, 1994
Phytanic acid alpha-oxidase deficiency (Refsum disease) presenting in infancy
M A Herbert, P T Clayton
Journal of Pediatric Gastroenterology and Nutrition
|
November 1, 1996
Sphincterotomy for jaundice in a neonate
M L Wilkinson, P T Clayton
Nutrition (Burbank, Los Angeles County, Calif.)
|
January 23, 1998
The role of phytosterols in the pathogenesis of liver complications of pediatric parenteral nutrition
P T Clayton, P Whitfield, K Iyer
Lancet (London, England)
|
January 14, 1978
Munchausen syndrome by proxy
P T Clayton, R Counahan, C Chantler
Journal of Inherited Metabolic Disease
|
January 1, 1992
Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate-deficient glycoprotein syndrome
P T Clayton, B G Winchester, G Keir
Biochemical Society Transactions
|
August 1, 1996
The use of automated electrospray ionization tandem MS for the diagnosis of inborn errors of metabolism from dried blood spots
A W Johnson, K Mills, P T Clayton
Rapid Communications in Mass Spectrometry : RCM
|
July 3, 1999
The identification of unusual bile acid metabolites by tandem mass spectrometry: use of low-energy collision-induced dissociation to produce informative spectra
H A Lemonde, A W Johnson, P T Clayton
Archives of Biochemistry and Biophysics
|
October 6, 2000
A new method for the analysis of urinary vitamin E metabolites and the tentative identification of a novel group of compounds
S A Pope, P T Clayton, D P Muller
Page
of 11
Search research articles
Search
Showing results (11-20 of 101) with videos related to
Sort By:
Page
of 11
Journal of Medical Genetics
|
July 1, 1988
Dysmorphic syndromes with demonstrable biochemical abnormalities
P T Clayton, E Thompson
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 19, 1980
A simplified gas-liquid chromatographic methods for the estimation of non-sulphated plasma bile acids
P T Clayton, D P Muller
Journal of Inherited Metabolic Disease
|
January 1, 1994
Phytanic acid alpha-oxidase deficiency (Refsum disease) presenting in infancy
M A Herbert, P T Clayton
Journal of Pediatric Gastroenterology and Nutrition
|
November 1, 1996
Sphincterotomy for jaundice in a neonate
M L Wilkinson, P T Clayton
Nutrition (Burbank, Los Angeles County, Calif.)
|
January 23, 1998
The role of phytosterols in the pathogenesis of liver complications of pediatric parenteral nutrition
P T Clayton, P Whitfield, K Iyer
Lancet (London, England)
|
January 14, 1978
Munchausen syndrome by proxy
P T Clayton, R Counahan, C Chantler
Journal of Inherited Metabolic Disease
|
January 1, 1992
Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate-deficient glycoprotein syndrome
P T Clayton, B G Winchester, G Keir
Biochemical Society Transactions
|
August 1, 1996
The use of automated electrospray ionization tandem MS for the diagnosis of inborn errors of metabolism from dried blood spots
A W Johnson, K Mills, P T Clayton
Rapid Communications in Mass Spectrometry : RCM
|
July 3, 1999
The identification of unusual bile acid metabolites by tandem mass spectrometry: use of low-energy collision-induced dissociation to produce informative spectra
H A Lemonde, A W Johnson, P T Clayton
Archives of Biochemistry and Biophysics
|
October 6, 2000
A new method for the analysis of urinary vitamin E metabolites and the tentative identification of a novel group of compounds
S A Pope, P T Clayton, D P Muller
Page
of 11