• Lipase, Urine
  • Methemoglobin Reductase, Blood
  • HLA Class I and II typing, Antigen or Genotyping
  • Prostatic Acid Phosphatase (PAP)
  • Metanephrines, Fractionated, 24 Hour, Urine
  • Phosphatidylserine Antibody, IgA, IgM, IgG
  • Clobazam, Urine
  • Addison's disease
  • Felty's syndrome
  • Calcitonin, Fine-Needle Aspiration Biopsy Needle Wash
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  • /Peutz-Jeghers Syndrome (STK11) Gene Mutation Analysis
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  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References

Peutz-Jeghers Syndrome (STK11) Gene Mutation Analysis
Medical Test

Clinical Utility
Access to Peutz-Jeghers Syndrome (STK11) Gene Mutation Analysis is restricted.