Phospholipid (Cardiolipin) Antibody, IgM
Acetoacetate (Ketones), Urine
Succinate Dehydrogenase (SDHA, SDHB, SDHC and SDHD) Gene Mutation Analysis
TGFB2 Gene Mutation Analysis
Fetal Fibronectin (fFN)
Acetylcholinesterase (AChE), Amniotic Fluid
Phosphorylated Tau 181 (pTau-181), Plasma
Cholesterol, Serum/Plasma
HLA-B75 (HLA-B*15:02) Genotyping for Carbamazepine Hypersensitivity
Cholesterol, Body Fluid

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/Medical Tests
/Williams Syndrome, 7q11.23 Deletion, FISH, Tissue

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

Williams Syndrome, 7q11.23 Deletion, FISH, Tissue
Medical Test

Clinical Utility

Access to Williams Syndrome, 7q11.23 Deletion, FISH, Tissue is restricted.