• Williams Syndrome, 7q11.23 Deletion
  • Lamotrigine, Serum
  • Coccidioides By Molecular Method, CSF
  • Ascorbic Acid (Vitamin C)
  • Galactose-1-phosphate Uridyltransferase (GALT) Gene Mutation Analysis
  • Lyme Disease (Borrelia burgdorferi), Molecular Detection, PCR
  • Endomysial (EMA) Antibody, IgA
  • 22q11.2 Deletion/Duplication, FISH
  • 1,3-Beta-D-Glucan (Fungitell® ß-D Glucan), CSF
  • IKBKAP (Inhibitor of Kappa Light Polypeptide Gene Enhancer in B-cells, Kinase Complex-associated Protein) Gene Mutation Analysis
  • LDS
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  • /Legius Syndrome (SPRED1) Sequencing
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  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

Legius Syndrome (SPRED1) Sequencing
Medical Test

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Access to Legius Syndrome (SPRED1) Sequencing is restricted.
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