Interleukin 6 (IL-6), Serum
Fragile X, FMR1 Gene Mutation Analysis
MAML2 (11q21) Rearrangement, Mucoepidermoid Carcinoma (MEC), FISH, Tissue
Chromosome Analysis, Solid Tumors
Iodine, Random, Urine
Hepatitis E Virus (HEV) RNA, Molecular, Quantitative
Phospholipid (Cardiolipin) Antibody, IgM
Idiopathic Pulmonary Fibrosis Diagnostic Test (Envisia™)
Methaqualone, Urine
Breast Cancer Antigen CA 15-3

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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.