• FoundationOne®CDx (F1CDx) and FoundationOne® Liquid CDx
  • Multiple Sclerosis Panel
  • Cytochrome P450 3A7 (CYP3A7) Genotyping
  • Glucose, Random, Urine
  • T-Cell Receptor Gene Rearrangement, Flow Cytometry, Bone Marrow
  • Jo 1 Antibody, IgG
  • Whole Exome Sequence Analysis, NGS
  • Hepatitis C Virus (HCV) Antibody
  • Reducing Substances (Sugars), Urine
  • Epstein-Barr Virus (EBV), Molecular Detection, Quantitative PCR
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /X-linked Intellectual Disability Gene Mutation Panel, NGS
  • 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

X-linked Intellectual Disability Gene Mutation Panel, NGS
Medical Test

Diseases (2)
Access to X-linked Intellectual Disability Gene Mutation Panel, NGS is restricted.