Serine and Arginine-rich Splicing Factor 2 (SRSF2) Gene Mutation Analysis
Coagulation Factor II Activity Assay, Plasma
Diabetes insipidus
Brucellosis
Rheumatic heart disease
Clonazepam, Serum
Biopsy, Bile Duct
Pepsinogen I
Cancer Antigen (CA) 72-4
Hypoxia-Inducible Factor Alpha (EPAS1/HIF2A) Gene, Exons 9 and 12 Sequencing

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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.