• Fragile X, FMR1 Gene Mutation Analysis
  • Prostaglandin D2 (PGD2), Serum
  • Prolactin
  • Vitamin K1
  • Colorado Tick Fever Virus Ab, IFA
  • Biopsy, Cervical
  • Epidermal Growth Factor Receptor (EGFR) Gene Mutation Analysis for Non-Small Cell Carcinoma of Lung
  • Hemoglobin, Qualitative, Urine
  • Maternal Serum Screen, First Trimester
  • Zaleplon, Urine
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
  • All
  • 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

CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
Medical Test

CPT
Access to CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2) is restricted.