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Results: 81 to 92 of 92

Tests names and labsConditionsGenes, analytes, and microbesMethods

Familial pyrimidinemia

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

DPYD

Division of Human Genetics Medical University Innsbruck
Austria
11
  • S Mutation scanning of the entire coding region

DPYD Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51314672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lysosomal Disorders NGS Panel

Fulgent Genetics
United States
186106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dihydropyrimidine Dehydrogenase (DPD) Gene Mutation Analysis

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
11
  • T Targeted variant analysis

Organic Acids, Comprehensive, Quantitative, Urine

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
4262
  • A Analyte

Dihydropyrimidin Dehydrogenase deficiency

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Toxicity to 5-fluorouracil (5-FU): DPYD gene and TYMS (2R / 2R, 2R / 3R o 3R / 3R) gene sequence analysis and genotype determination

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
12
  • C Sequence analysis of the entire coding region

Dihydropyrimidine Dehydrogenase Deficiency

Bioscientia GmbH Center for Human Genetics
Germany
11
  • T Targeted variant analysis

Dihydropyrimidine Dehydrogenase Deficiency

Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD
Netherlands
11
  • A Analyte
  • E Enzyme assay
  • C Sequence analysis of the entire coding region

Results: 81 to 92 of 92

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.