• Klippel-Trenaunay Syndrome
  • SLCO1B3 Gene Mutation Analysis
  • Steroid Sulfatase Gene, Xp22.3 Deletion, FISH
  • Biopsy, Breast (Core Needle Biopsy/Fine Needle Aspiration)
  • Fluphenazine, Serum
  • MYH7 Gene Mutation Analysis
  • Influenza Virus Type A and B, Culture
  • Biopsy, Nerve
  • Hematolymphoid Neoplasm Gene Mutation Panel, NGS
  • Mercury, Random, Urine
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Chromosome Breakage Study, Chorionic Villi
  • 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

Chromosome Breakage Study, Chorionic Villi
Medical Test

Methodology
Access to Chromosome Breakage Study, Chorionic Villi is restricted.