Culture, Pleural Fluid
Hereditary Hemorrhagic Telangiectasia, Gene Mutation Panel
MAML2 (11q21) Rearrangement, Mucoepidermoid Carcinoma (MEC), FISH, Tissue
Transferrin Receptor, Soluble
Lysosomal Acid Lipase, Enzyme Activity
Nordiazepam, Urine
C1 Esterase Inhibitor, Functional Assay
Coagulation Factor VIII Inhibitor Screen, Plasma
Ehrlichia and Anaplasma Blood Smear
Coagulation Factor VII Activity Assay, Plasma

LDS
Sign up
Log in

LDS
/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.