• Adenovirus DNA, Real-Time PCR, Quantitative
  • Duodenal Mucosal Biopsy, Endoscopic
  • Becker muscular dystrophy
  • Galactose-1-phosphate Uridyltransferase (GALT) Gene Mutation Analysis
  • Smooth Muscle Antibody
  • Neuron-Specific Enolase (NSE), Serum
  • Triazolam, Urine
  • Cardiac arrest
  • Fibrinogen Antigen
  • Thyroid hormone uptake (T Uptake)
  • 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

Additional ICD10
Access to Chromosome Analysis, for Congenital Disorders, Blood is restricted.