Mitochondrial M2 Antibody, IgG
Sodium, Random, Urine
Serine and Arginine-rich Splicing Factor 2 (SRSF2) Gene Mutation Analysis
Mercury, Blood
Fungal Culture, Toenail
Antinuclear Antibody (ANA), IFA Patterning
Serotonin Receptor HTR2A Genotyping
Histamine, 24-Hour Urine
Avantect Pancreatic Cancer Test
Duchenne/Becker Muscular Dystrophy (DMD) Gene Mutation Analysis

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/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

Clinical Utility

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