Human Papillomavirus (HPV), High-Risk, DNA In Situ Hybridization
Thrombin Time
Hypertrophic Cardiomyopathy Gene Mutation Panel, NGS
Squamous Cell Carcinoma Antigen (SSCA)
Biopsy, Different Sites
Tropheryma whipplei, Molecular
Peutz-Jeghers Syndrome (STK11) Gene Mutation Analysis
Bordetella pertussis Antibody, IgA, IgG
Lysosomal Acid Lipase, Gene Variation
Hereditary Dilated Cardiomyopathy Gene Mutation Panel, NGS

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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

Specimen Collection

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