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E Treacy

Showing results (11-20 of 16) with videos related to

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Chemical Research in Toxicology|August 1, 1997
Human flavin-containing monooxygenase form 3: cDNA expression of the enzymes containing amino acid substitutions observed in individuals with trimethylaminuriaJ R Cashman, Y A Bi, J Lin, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Maple syrup urine disease: interrelations between branched-chain amino-, oxo- and hydroxyacids; implications for treatment; associations with CNS dysmyelinationE Treacy, C L Clow, T R Reade, et al.
The Journal of Pediatrics|September 1, 1996
Glutathione deficiency as a complication of methylmalonic acidemia: response to high doses of ascorbateE Treacy, L Arbour, P Chessex, et al.
Journal of Medical Genetics|January 1, 1996
Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humansE Treacy, C Polychronakos, M Vekemans, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Mutation at the phenylalanine hydroxylase gene (PAH) and its use to document population genetic variation: the Quebec experienceK C Carter, S Byck, P J Waters, et al.
American Journal of Human Genetics|January 1, 1995
Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in EuropeansR C Eisensmith, A A Goltsov, C O'Neill, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Chemical Research in Toxicology|August 1, 1997
Human flavin-containing monooxygenase form 3: cDNA expression of the enzymes containing amino acid substitutions observed in individuals with trimethylaminuriaJ R Cashman, Y A Bi, J Lin, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Maple syrup urine disease: interrelations between branched-chain amino-, oxo- and hydroxyacids; implications for treatment; associations with CNS dysmyelinationE Treacy, C L Clow, T R Reade, et al.
The Journal of Pediatrics|September 1, 1996
Glutathione deficiency as a complication of methylmalonic acidemia: response to high doses of ascorbateE Treacy, L Arbour, P Chessex, et al.
Journal of Medical Genetics|January 1, 1996
Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humansE Treacy, C Polychronakos, M Vekemans, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Mutation at the phenylalanine hydroxylase gene (PAH) and its use to document population genetic variation: the Quebec experienceK C Carter, S Byck, P J Waters, et al.
American Journal of Human Genetics|January 1, 1995
Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in EuropeansR C Eisensmith, A A Goltsov, C O'Neill, et al.
Pageof 2