• Zinc Finger CCCH-type, RNA Binding Motif and Serine/arginine-rich 2 (ZRSR2) Gene Mutation Analysis
  • Melanoma, FISH, Tissue
  • Actinomyces, Molecular Method
  • Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
  • Brucella Antibody, IgG and IgM
  • Biopsy, Blood Vessel
  • Thalassemia and Hemoglobinopathy Evaluation
  • Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
  • Aldosterone, Urine
  • Adenovirus DNA, Real-time PCR, Qualitative
  • LDS
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  • /X-linked Intellectual Disability Gene Mutation Panel, NGS
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  • 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

Methodology
Access to X-linked Intellectual Disability Gene Mutation Panel, NGS is restricted.