• Williams Syndrome, 7q11.23 Deletion, FISH, Tissue
  • Vascular Endothelial Growth Factor (VEGF)
  • Gentamicin, Peak, Serum
  • Human Platelet Antigen 1 (HPA-1) Genotyping
  • Pheochromocytoma
  • MSH2 Gene Mutation Analysis (Known Mutations, Duplication/Deletion/Sequencing)
  • Hydroxyzine, Serum
  • MLH1 Hypermethylation (Promoter Methylation) Analysis, Tissue
  • T Cell Lymphoma, FISH, Bone Marrow
  • RET Gene Rearrangements by FISH
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /NHP2 Gene Mutation Analysis
  • 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

NHP2 Gene Mutation Analysis
Medical Test

CPT
Access to NHP2 Gene Mutation Analysis is restricted.