• Carnitine-Acylcarnitine Translocase Deficiency, Gene Mutation Analysis
  • Diphenhydramine, Urine
  • Amylase, Body Fluid
  • Lactate Dehydrogenase (LDH), Serum
  • Salivary Gland Tumor, MYB (6q23) Rearrangement by FISH
  • Methamphetamine, Urine
  • Phospholamban (PLN) Gene Mutation Analysis
  • Miller-Dieker Syndrome, 17p13.3 Deletion, FISH
  • Imipramine, Serum
  • Vascular Endothelial Growth Factor (VEGF)
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  • /Severe Combined Immunodeficiency Gene 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

Severe Combined Immunodeficiency Gene Panel, NGS
Medical Test

Methodology
Access to Severe Combined Immunodeficiency Gene Panel, NGS is restricted.
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