Primary Hyperoxaluria Gene Mutation Panel
Respiratory Pathogen (Pneumonia) Panel with Antibiotic Resistance Genes, Molecular
Transthyretin (TTR) Gene Mutation Analysis
Renin Activity
Valproic Acid, Free and Total, Serum
Inhibin A
Influenza Virus Type A and B, PCR
15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
Valproic Acid, Free, Serum
Alprazolam, 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

Clinical Utility

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