Williams Syndrome, 7q11.23 Deletion, FISH, CV
HLA-B75 (HLA-B*15:02) Genotyping for Carbamazepine Hypersensitivity
Glycogen storage disease type II (Pompe disease)
Aquaporin-4 (AQP4) Antibody, IgG, Cell-Binding-IFA Assay, Serum
Mumps Virus Antibody, IgG
Beta-Glucuronidase, Blood
Neonatal group B Streptococcus infection
VDRL Test, CSF
Proteinase 3 Antibody, IgG
Trisomy 13 (Patau syndrome)
LDS
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All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Culture, Stool
Medical Test
Additional Testing
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