Primary Hyperoxaluria Gene Mutation Panel
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

Biopsy, Blood Vessel
Medical Test

Access to Biopsy, Blood Vessel is restricted.