• Biopsy, Kidney
  • SARS-CoV-2 (COVID-19) Coronavirus, Molecular
  • Synovial Sarcoma Gene Mutation Panel, NGS
  • Duchenne/Becker Muscular Dystrophy (DMD) Gene Mutation Analysis
  • Cortisol, Free, Serum
  • Acid Sphingomyelinase Activity
  • Oxymorphone, Urine
  • Apolipoprotein E (Apo E) Genotyping
  • Hemoglobin F (Fetal Hemoglobin)
  • Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Williams Syndrome, 7q11.23 Deletion, FISH, Amniotic Fluid
  • 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

Williams Syndrome, 7q11.23 Deletion, FISH, Amniotic Fluid
Medical Test

ICD10
Access to Williams Syndrome, 7q11.23 Deletion, FISH, Amniotic Fluid is restricted.