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Results: 1 to 5 of 5

Tests names and labsConditionsGenes, analytes, and microbesMethods

Smith-Lemli-Opitz Screen, Plasma

Mayo Clinic Laboratories Mayo Clinic
United States
12
  • A Analyte

CentoMetabolic MOx

Centogene US, LLC - The Rare Disease Company
United States
195221
  • A Analyte
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoMetabolic MOx

Centogene AG - the Rare Disease Company
Germany
195221
  • A Analyte
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Plasma/Serum 7-Dehydrocholesterol

Sterol Analysis Laboratory Oregon Health and Science University
United States
11
  • A Analyte

Smith-Lemli-Opitz Syndrome

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

Results: 1 to 5 of 5

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.