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Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

Apolipoprotein B Deficiency, Mutation (p.Arg3500Gln) APOB Gene

Reference Laboratory Genetics
Spain
11
  • E Sequence analysis of select exons

Apolipoprotein B Deficiency , Mutations (p.Arg3500Gln,p.Arg3500Trp,p.His3543Tyr) APOB Gene

Reference Laboratory Genetics
Spain
11
  • E Sequence analysis of select exons

Hypercholesterolemia, autosomal dominant, type B

Labor Dr. Wisplinghoff
Germany
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Hypercholesterolemia, due to ligand-defective apo B

MedGene
Slovakia
11
  • E Sequence analysis of select exons

Hypercholesterolemia, due to ligand-defective apo B

Praxis fuer Humangenetik Wien
Austria
11
  • E Sequence analysis of select exons

Familial Hypercholesterolemia Type B (APOB, FDB)

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • E Sequence analysis of select exons

Results: 1 to 6 of 6

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.