• Arylsulfatase A, 24 Hour, Urine
  • Fibroblast Growth Factor Receptor 1 (FGFR1), 8p11.2 Rearrangement, FISH, Bone Marrow
  • Corticosterone, Serum
  • Fungal Culture, Body Fluid
  • Red Blood Cell Antigen Genotyping (Immucor PreciseType, BLOODchip® ID CORE XT™)
  • Lamotrigine, Serum
  • Bordetella Pertussis Antibody, IgA
  • Ewing Sarcoma (EWSR1/FLI1 and EWSR1/ERG) by Reverse Transcriptase PCR (RT-PCR), Paraffin
  • B-cell Activating Factor Receptor (BAFF-R) Gene Mutation Analysis
  • CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
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  • /Medical Tests
  • /Metabolic Storage Disease Gene Mutation Panel, NGS
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  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
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  • Additional Testing
  • Turnaround Time
  • CPT
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  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

Metabolic Storage Disease Gene Mutation Panel, NGS
Medical Test

Turnaround Time
Access to Metabolic Storage Disease Gene Mutation Panel, NGS is restricted.