• Sarcoma Gene Mutation, Fusion and Rearrangement Panel, NGS
  • Interferon Lambda 3 (IFNL3) Gene Mutation Analysis
  • Maternal Serum Screen, First Trimester
  • Catecholamine Fractionation, Plasma
  • Fibrinogen Antigen
  • NOTCH3 (CADASIL) Gene Mutations Analysis
  • Culture, Acid-Fast Bacilli, Urine
  • Reticulocyte Count
  • Oligoclonal Bands, Serum
  • RET Gene Rearrangements by FISH
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Chromosome Analysis, for Congenital Disorders, Blood
  • 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 Analysis, for Congenital Disorders, Blood
Medical Test

References
Access to Chromosome Analysis, for Congenital Disorders, Blood is restricted.