• Williams Syndrome, 7q11.23 Deletion, FISH, Amniotic Fluid
  • Alkaline Phosphatase Isoenzymes
  • Legius Syndrome (SPRED1) Sequencing
  • Anemia Panel
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  • SMAD4 Germline Mutation Analysis
  • Thyroid hormone uptake (T Uptake)
  • Hydroxyzine, Serum
  • Biopsy, Thymus
  • Plasminogen Activator Inhibitor Antigen, Plasma
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  • /Noonan Spectrum Disorders Gene Mutation Panel, NGS
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  • Additional ICD10
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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

Noonan Spectrum Disorders Gene Mutation Panel, NGS
Medical Test

Additional ICD10
Access to Noonan Spectrum Disorders Gene Mutation Panel, NGS is restricted.