Thrombin Time
Squamous Cell Carcinoma Antigen (SSCA)
Tropheryma whipplei, Molecular
Peutz-Jeghers Syndrome (STK11) Gene Mutation Analysis
Parathyroid Hormone Related Protein
Lysosomal Acid Lipase, Gene Variation
Hereditary Dilated Cardiomyopathy Gene Mutation Panel, NGS
Multiple Sclerosis Panel
Usher Syndrome
Decipher Bladder Cancer Genomic Profiling

LDS
Sign up
Log in

LDS
/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.