• Electrophoresis, Protein, 24 Hour, Urine
  • Severe Combined Immunodeficiency Gene Panel, NGS
  • Vanillylmandelic Acid (VMA) and Homovanillic Acid (HVA), Random, Urine
  • Methemoglobin
  • Common Variable Immunodeficiency Confirmation Panel, Flow
  • Idiopathic and Hereditary Pancreatitis
  • Cytochrome P450 1A2 (CYP1A2) Genotyping
  • Selenium, 24 Hour, Urine
  • Carcinoembryonic Antigen (CEA), Pleural Fluid
  • Cardiac Ion Channelopathies Multi-Gene Panel, NGS
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  • /von Willebrand Disease 2N (Subtype Normandy), Genotyping
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  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References

von Willebrand Disease 2N (Subtype Normandy), Genotyping
Medical Test

Clinical Utility
Access to von Willebrand Disease 2N (Subtype Normandy), Genotyping is restricted.
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