Fibrinogen Degradation Products (DR-70®)
Lyme Disease (Borrelia burgdorferi) Confirmatory Testing
Infectious Mononucleosis Screen (Mono Test)
Macroprolactin, Serum
Paroxysmal Nocturnal Hemoglobinuria (PNH) (CD55, CD59), Flow, Blood
LAMP2 Gene Mutation Analysis
Human Papillomavirus (HPV), Low-Risk, DNA In Situ Hybridization
Rickettsia rickettsii DNA, Real-Time PCR
Parvovirus B19 Antibody, IgG and IgM
Culture, Leptospira

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/Medical Tests
/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.