Methylphenidate, Urine
Pregnenolone
Williams Syndrome, 7q11.23 Deletion, FISH, Tissue
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

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LDS
/Medical Tests
/Noonan Spectrum Disorders Gene Mutation Panel, NGS

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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

Noonan Spectrum Disorders Gene Mutation Panel, NGS
Medical Test

Turnaround Time

Access to Noonan Spectrum Disorders Gene Mutation Panel, NGS is restricted.