Human Epididymis Protein 4 (HE4)
EsoGuard Methylation Assay for Barrett’s Esophagus
Tobramycin, Trough, Serum
Herpes Simplex Virus (HSV) 1 and 2 IgG
Amobarbital, Urine
CaM Kinase II (CaMKII, Calcium-dependent Calmodulin Protein Kinase II) Activation
Adenovirus DNA, Real-Time PCR, Quantitative
Buspirone, Urine
NOTCH3 (CADASIL) Gene Mutations Analysis
Bismuth, Blood
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
Additional Testing
Access to
CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
is restricted.
Sign up now