• Blastomyces Antibody, Spinal Fluid
  • Phencyclidine (PCP), Serum
  • 5-hydroxytryptamine receptor 1A (HTR1A)
  • D-Xylose Absorption Test
  • BCR-ABL Translocation by RT-PCR, Quantitative, Bone Marrow
  • Hereditary Hemorrhagic Telangiectasia, Gene Mutation Panel
  • Asparagus, IgE
  • Metanephrines, Fractionated, 24 Hour, Urine
  • Polyoma BK Virus, PCR, Quantitative, Plasma
  • ASXL1 Gene Mutation Analysis
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS
Medical Test

Diseases (17)
Access to Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS is restricted.
Loading...