Copper, 24 Hour, Urine
Hereditary Hemolytic Anemia Gene Mutation Panel, NGS
Monoclonal Protein Study, 24 Hour, Urine
Malaria, Molecular Detection, PCR
Beta-Glucuronidase, Fibroblasts
MAML2 (11q21) Rearrangement, Mucoepidermoid Carcinoma (MEC), FISH, Tissue
Complete Autoimmune Disease Panel
Legionella pneumophila Antibody, IgG by IFA
Protein Immunofixation Electrophoresis, Serum
Bone Alkaline Phosphatase, Serum
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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
References
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CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
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