• HLA-B27 Genotyping for Uveitis
  • Gram Stain with the Nugent Scoring
  • Serotonin, Serum
  • HLA-B51 Genotyping for Behçet’s Disease
  • Lead, Random, Urine
  • AIRE gene mutation
  • Biopsy, Cervical
  • Endomysial (EMA) Antibody, IgG
  • Central Nervous System (Meningitis/Encephalitis) Pathogen Panel, Molecular Method
  • Thyroglobulin, Fine Needle Aspiration (FNA)
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /TNF receptor superfamily member 13B Gene Mutation Analysis
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References

TNF receptor superfamily member 13B Gene Mutation Analysis
Medical Test

Specimen Collection
Access to TNF receptor superfamily member 13B Gene Mutation Analysis is restricted.
Loading...