• 22q11.2 deletion syndrome
  • 22q11.2 microdeletion (DiGeorge) syndrome
  • Williams Syndrome, 7q11.23 Deletion, FISH, CV
  • Male infertility
  • Primary ovarian insufficiency
  • Seizure disorder
  • Dysfunctional uterine bleeding
  • Gastrointestinal stromal tumor
  • Benign neoplasm, ovary
  • Dementia With Lewy Bodies
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Prader-Willi and Angelman Syndrome Molecular Analysis
  • 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

Prader-Willi and Angelman Syndrome Molecular Analysis
Medical Test

Additional ICD10
Access to Prader-Willi and Angelman Syndrome Molecular Analysis is restricted.