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Products found: 123Search results

University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases

Disorder Genes Test Method Lab Info Product code  
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Rhizomelic Chondrodysplasia Punctata Type 2 GNPAT, Enzyme assay
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Rhizomelic Chondrodysplasia Punctata Type 2 GNPAT, Sequence analysis of the entire coding region
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Rhizomelic Chondrodysplasia Punctata Type 3 AGPS, Sequence analysis of the entire coding region
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Short Chain Acyl-CoA Dehydrogenase Deficiency ACADS, Analyte
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Short Chain Acyl-CoA Dehydrogenase Deficiency ACADS, Enzyme assay
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Short Chain Acyl-CoA Dehydrogenase Deficiency ACADS, Sequence analysis of the entire coding region
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Sjogren-Larsson Syndrome ALDH3A2, Enzyme assay
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Sjogren-Larsson Syndrome ALDH3A2, Sequence analysis of the entire coding region
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Smith-Lemli-Opitz Syndrome DHCR7, Analyte
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Smith-Lemli-Opitz Syndrome DHCR7, Sequence analysis of the entire coding region
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases SUCLA2-Related Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form, with Mild Methylmalonic Aciduria SUCLA2, Analyte
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases SUCLA2-Related Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form, with Mild Methylmalonic Aciduria SUCLA2, Enzyme assay
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