X-linked Intellectual Disability Gene Mutation Panel, NGS
Zinc Finger CCCH-type, RNA Binding Motif and Serine/arginine-rich 2 (ZRSR2) Gene Mutation Analysis
Melanoma, FISH, Tissue
Actinomyces, Molecular Method
Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
Brucella Antibody, IgG and IgM
Biopsy, Blood Vessel
Thalassemia and Hemoglobinopathy Evaluation
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
Aldosterone, Urine

Complement Component CH50
Medical Test

Access to Complement Component CH50 is restricted.