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S E Olpin

Showing results (21-30 of 25) with videos related to

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Journal of Inherited Metabolic Disease|September 10, 2005
Ornithine aminotransferase deficiency: diagnostic difficulties in neonatal presentationM A Cleary, L Dorland, T J de Koning, et al.
Journal of Medical Genetics|January 8, 2008
Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutationsH A L Tuppen, F Fattori, R Carrozzo, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Features of carnitine palmitoyltransferase type I deficiencyS E Olpin, J Allen, J R Bonham, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiencyS E Olpin, S Clark, B S Andresen, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyS E Olpin, A Afifi, S Clark, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Journal of Inherited Metabolic Disease|September 10, 2005
Ornithine aminotransferase deficiency: diagnostic difficulties in neonatal presentationM A Cleary, L Dorland, T J de Koning, et al.
Journal of Medical Genetics|January 8, 2008
Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutationsH A L Tuppen, F Fattori, R Carrozzo, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Features of carnitine palmitoyltransferase type I deficiencyS E Olpin, J Allen, J R Bonham, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiencyS E Olpin, S Clark, B S Andresen, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyS E Olpin, A Afifi, S Clark, et al.
Pageof 3