West Nile Virus (WNV) Antibody, IgG and IgM
Vascular Endothelial Growth Factor (VEGF)
Cystic Fibrosis (CFTR) Gene Mutation Analysis
Bilirubin Total, Serum
Sodium Voltage-gated Channel Alpha Subunit 1 (SCN1A) Gene Mutation Analysis
Chromosome Analysis, Hematologic Disorders, Blood
Chronic Lymphocytic Leukemia (CLL), FISH, Blood
Adenovirus Antibody
Follicular Lymphoma, bcl-2/JH t(14;18), FISH
Catecholamine Fractionation, Plasma

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

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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

Reference Ranges

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