Malaria, Molecular Detection, PCR
Hereditary Hemolytic Anemia Gene Mutation Panel, NGS
Complete Autoimmune (Connective Tissue Autoimmune) Disease Panel
Legionella pneumophila Antibody, IgG by IFA
Copper, 24 Hour, Urine
Beta-Glucuronidase, Fibroblasts
Monoclonal Protein Study, 24 Hour, Urine
Spondylosis and associated disorders
Schizophrenia
Malignant neoplasm, adrenal gland
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
References
Access to
CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
is restricted.
Sign up now