Smith-Magenis/Potocki-Lupski Syndromes, 17p11.2 Deletion/Duplication, FISH
Corynebacterium diphtheriae, Culture
Prenatal Aneuploidy Detection, FISH
Aspergillus DNA, Qualitative, Real-Time PCR, BAL
Cardio inCode-Score for Cardiovascular Risk Assessment (GENinCode)
Cerebrospinal Fluid Microscopic Evaluation, Cell Count and Differentiation
Coccidioides Antibody, IgG
Triiodothyronine (T3), Free
Antibody Identification, Erythrocytes
Ehlers-Danlos Syndrome Gene Mutation Panel, NGS
LDS
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Spinocerebellar Ataxia Type 2 (ATXN2) 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
Spinocerebellar Ataxia Type 2 (ATXN2) Gene Mutation Analysis
Medical Test
Interpretation
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Spinocerebellar Ataxia Type 2 (ATXN2) Gene Mutation Analysis
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