Comprehensive Hereditary Cancer Panel, NGS
Interleukin 2 Receptor Subunit Gamma (IL2RG) Genotyping
Arrhythmogenic Cardiomyopathy Gene Mutation Panel, NGS
Monoclonal Gammopathy of Undetermined Significance (MGUS)
Phencyclidine (PCP), Urine
Toxoplasma Gondii IgG and IgM, CSF
Tumor Necrosis Factor Receptor-Ass Periodic Syndrome (TNFRSF1A) Gene Mutation Analysis
Epidermal Growth Factor Receptor (EGFR) Gene Mutation Analysis
Branched-Chain Amino Acids for Maple Syrup Disease Monitoring
Thermoactinomyces vulgaris, Antibody, IgG
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Spinocerebellar Ataxia Type 1 (ATXN1) 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 1 (ATXN1) Gene Mutation Analysis
Medical Test
Diseases (3)
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Spinocerebellar Ataxia Type 1 (ATXN1) Gene Mutation Analysis
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