• Monoclonal Protein Study, Random, Urine
  • JAK2 Gene Mutation (Exons 12-15 or full sequencing) Analysis
  • Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene Mutation Analysis
  • Immunoglobulin Heavy and Light Chain (HLC) Pairs, IgG Kappa and IgG Lambda
  • Protein C, Total Antigen
  • Antiphospholipid syndrome
  • Behçet’s disease (Behcet syndrome)
  • Mucolipidosis type IV
  • Rubella Antibody IgG and IgM
  • Enterobiasis
  • LDS
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  • /Hereditary Erythrocytosis Gene Mutation Panel, NGS
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  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

Hereditary Erythrocytosis Gene Mutation Panel, NGS
Medical Test

Diseases (1)
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