Hexosaminidase A (HEXA) Gene Mutation Analysis
Heparin Induced Antibody
Rapid Plasma Reagin (RPR), Serum
Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Gene Mutation Analysis
Potassium, Random, Urine
Tumor Suppressor Gene P53 (TP53) Gene Mutation Analysis, Li-Fraumeni Syndrome
B and T Cell Gene Rearrangement, Blood
Cytochrome P450 4F2 (CYP4F2) Genotyping

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

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References

Williams Syndrome, 7q11.23 Deletion
Medical Test

Additional Testing

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