ADAMTS13 Activity and Inhibitor Assay
Epidermolysis bullosa acquisita (EBA)
Beta-Glucuronidase, Fibroblasts
Lysosomal Acid Lipase, Enzyme Activity
Enterovirus, Real-time PCR, Plasma
Staphylococcus aureus and Staph Methicillin-Resistant (MRSA) by Molecular Method
Temazepam, Urine
B-Cell Lymphoma, FISH, Bone Marrow
Loeys-Dietz syndrome
Measles (Rubeola) Antibody, IgM
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
Specimen Collection
Access to
CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
is restricted.
Sign up now