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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 Zellweger Syndrome Spectrum PEX1, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, Sequence analysis of the entire coding region
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Zellweger Syndrome Spectrum PEX1, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, Enzyme assay
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Zellweger Syndrome Spectrum PEX1, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, Analyte
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Very Long Chain Acyl-Coenzyme A Dehydrogenase Deficiency ACADVL, Sequence analysis of the entire coding region
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Very Long Chain Acyl-Coenzyme A Dehydrogenase Deficiency ACADVL, Enzyme assay
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Very Long Chain Acyl-Coenzyme A Dehydrogenase Deficiency ACADVL, Analyte
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Tyrosine Hydroxylase Deficiency TH, Sequence analysis of the entire coding region
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Tyrosine Hydroxylase Deficiency TH, Analyte
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Trifunctional Protein Deficiency HADHB, Sequence analysis of the entire coding region
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Trifunctional Protein Deficiency HADHB, Enzyme assay
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Trifunctional Protein Deficiency HADHB, Analyte
University of Amsterdam Academic Medical Center, Laboratory Genetic Metabolic Diseases Systemic Primary Carnitine Deficiency SLC22A5, Sequence analysis of the entire coding region
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