• Coagulation Factor VII Activity Assay, Plasma
  • Cimetidine, Urine
  • Ehrlichia and Anaplasma Blood Smear
  • Helicobacter pylori, Urea Breath Test
  • Duodenal Mucosal Biopsy, Endoscopic
  • Hypobetalipoproteinemia
  • Ethosuximide, Urine
  • CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
  • Vitamin K1
  • Subcutaneous Fat Aspirate
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Factor XIII (F13A1) V34L Genetic Variation 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

Factor XIII (F13A1) V34L Genetic Variation Analysis
Medical Test

Diseases (2)
Access to Factor XIII (F13A1) V34L Genetic Variation Analysis is restricted.