Desmethylclomipramine, Urine
Cotinine, Urine
Ethosuximide, Serum
Muscular Dystrophies Gene Mutation Panel, NGS
Ascorbic Acid (Vitamin C)
Hematolymphoid Neoplasm Gene Mutation Panel, NGS
Primidone, Urine
Cortisol, Free and Total, Serum
Runt Related Transcription Factor 1 (RUNX1) Gene Mutation Analysis
Cytomegalovirus (CMV) Antibody, IgM

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LDS
/Medical Tests
/Prader-Willi and Angelman Syndrome Molecular Analysis

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

Prader-Willi and Angelman Syndrome Molecular Analysis
Medical Test

Reference Ranges

Access to Prader-Willi and Angelman Syndrome Molecular Analysis is restricted.