Hereditary Hemolytic Anemia Gene Mutation Panel, NGS
Gastrointestinal Stromal Tumor Gene Mutation Panel, NGS
Soluble Fibrin Monomer
Treponema pallidum Antibody, FTA-ABS, IgG, CSF
Diphenhydramine, Urine
IgG Subclasses
Peripheral Myelin Protein 22 (PMP22), Peripheral Neuropathy, FISH
SERPINA1 Gene Mutation Analysis
Blastomyces Antibody, Spinal Fluid
Protein, Total, Serum

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/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

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