Interleukin 6 (IL-6), Serum
MUTYH Gene Mutation Analysis (Y165C and G382D) for MUTYH associated polyposis (MAP)
Hereditary Hemorrhagic Telangiectasia, Gene Mutation Panel
Fragile X, FMR1 Gene Mutation Analysis
Iodine, Random, Urine
Lysosomal Acid Lipase, Enzyme Activity
Transferrin Receptor, Soluble
Chromosome Analysis, Solid Tumors
Phospholipid (Cardiolipin) Antibody, IgM
Phospholipase A2 Receptor (PLA2R) Antibody, IgG

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/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

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