G6PC (Glucose-6-phosphatase, Catalytic Subunit), Glycogen Storage Disease Type 1 (von Gierke Disease) Gene Mutation Analysis
CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
Products of Conception (POC) Aneuploidy Detection, FISH, Tissue
Lupus nephritis
Thyroid Stimulating Immunoglobulin (TSI)
Renin Activity
Transthyretin (TTR) Gene Mutation Analysis
Valproic Acid, Free and Total, Serum
Alprazolam, Serum
Insulin-Like Growth Factor Binding Protein 3 (IGFBP-3)
LDS
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Primary Hyperoxaluria Gene Mutation Panel
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
Primary Hyperoxaluria Gene Mutation Panel
Medical Test
Diseases (1)
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Primary Hyperoxaluria Gene Mutation Panel
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