• Citalopram, Serum
  • AIP gene mutation analysis
  • Splicing Factor 3b Subunit B1 (SF3B1) Gene Mutation Analysis
  • Measles (Rubeola) Virus Culture
  • Babesia microti, Molecular
  • Complement Component C4
  • Chromosome Breakage Study, Chorionic Villi
  • Beta-2 Transferrin, CSF
  • Alpha 2 Plasmin Inhibitor, Plasma
  • Allergen Specific IgE, Mold (Allergens) Panel
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /1p36.3 Microdeletion Syndrome, FISH
  • 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

1p36.3 Microdeletion Syndrome, FISH
Medical Test

Additional ICD10
Access to 1p36.3 Microdeletion Syndrome, FISH is restricted.