Complement Component C4
Cerebrospinal Fluid Microscopic Evaluation, Cell Count and Differentiation
17-Hydroxyprogesterone, Amniotic fluid
1p36.3 Microdeletion Syndrome, FISH
PDGFRB/TEL Translocation (5;12) for Chronic Myelomonocytic Leukemia, FISH, Bone Marrow
Organic Acids, Urine
Zinc, 24 Hour, Urine
Mumps Virus Antibody, IgM
Carcinoembryonic Antigen (CEA), Pancreatic Cyst Fluid
Hereditary Neuroendocrine Tumor Gene Mutation Panel, NGS
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Spinobulbar Muscular Atrophy (Kennedy Disease), Androgen Receptor Gene Mutation Analysis
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
Spinobulbar Muscular Atrophy (Kennedy Disease), Androgen Receptor Gene Mutation Analysis
Medical Test
CPT
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Spinobulbar Muscular Atrophy (Kennedy Disease), Androgen Receptor Gene Mutation Analysis
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