Aspergillus DNA, Qualitative, Real-Time PCR, Sputum
Calcium Channel Voltage-dependent L Type alpha 1S Subunit (CACNA1S) Gene Mutation Analysis
Oxycodone, Serum
Copper, 24 Hour, Urine
Pheniramine, Urine
Mucopolysaccharidosis VI (ARSB) Gene Mutation Analysis
Biopsy, Mediastinal Lymph Node
Cystatin C, Serum
Schistosoma, Antibody, IgG
Obsessive-compulsive disorder

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

Additional ICD10

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