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L Thuillier

Showing results (31-40 of 33) with videos related to

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Neuromuscular Disorders : NMD|March 29, 2000
Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patientL Thuillier, C Sevin, F Demaugre, et al.
Molecular Genetics and Metabolism|May 15, 2001
Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite communityC Prip-Buus, L Thuillier, N Abadi, et al.
Molecular Genetics and Metabolism|May 15, 2001
Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening programC Prasad, J P Johnson, J P Bonnefont, et al.
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Showing results (31-40 of 33) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 33 results.
Neuromuscular Disorders : NMD|March 29, 2000
Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patientL Thuillier, C Sevin, F Demaugre, et al.
Molecular Genetics and Metabolism|May 15, 2001
Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite communityC Prip-Buus, L Thuillier, N Abadi, et al.
Molecular Genetics and Metabolism|May 15, 2001
Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening programC Prasad, J P Johnson, J P Bonnefont, et al.
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