Subtelomeric Region Anomalies, FISH, Amniotic Fluid
Epstein-Barr Virus (EBV) Nuclear Antigen (EBNA) Antibody, IgG
Clobazam, Serum
U2 Small Nuclear RNA Auxiliary Factor 1 (U2AF1) Gene Mutation Analysis
11-Deoxycortisol, Quantitative, Serum
Multiple Sulfatase Deficiency, Gene Mutation Analysis
Adenovirus Antigen Detection
Clostridium difficile (C. Diff), Culture
Leukemia/Lymphoma Immunophenotyping by Flow Cytometry, Tissue
Aortic Dysfunction or Dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome type IV, arterial tortuosity syndrome) Gene Mutation Panel, NGS
LDS
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DMPK Gene Analysis for Myotonic Dystrophy Type I (DM1)
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
DMPK Gene Analysis for Myotonic Dystrophy Type I (DM1)
Medical Test
Additional Testing
Access to
DMPK Gene Analysis for Myotonic Dystrophy Type I (DM1)
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