Comprehensive Epilepsy Gene Mutation Panel, NGS
Hemoglobin A1c
FLT3 (FMS-related Tyrosine Kinase 3) Mutation Analysis, Blood
Otitis media
Trisomy 18 (Edwards syndrome)
Myotonic dystrophy
Crohn's disease
Bacterial Culture, Upper Respiratory
CaM Kinase II (CaMKII, Calcium-dependent Calmodulin Protein Kinase II) Activation
Friedreich's ataxia

Dexedrine (Dextroamphetamine), Urine
Medical Test

Access to Dexedrine (Dextroamphetamine), Urine is restricted.