Peripheral Myelin Protein 22 (PMP22), Peripheral Neuropathy, FISH
JAK2 (V617F) Gene Mutation Analysis
Imipramine, Serum
Bone Marrow Aspiration
Comprehensive Pharmacogenetics (PGx) Gene Variation Panel
COL3A1 Genes Variations Analysis
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutation Analysis
CDKN1C Gene Mutation Analysis
Herpes Simplex Virus (HSV) 1 and 2 by PCR
Actin (Smooth Muscle) Antibody, IgG

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/Medical Tests
/Chromosome Analysis, for Congenital Disorders, Blood

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

Chromosome Analysis, for Congenital Disorders, Blood
Medical Test

Turnaround Time

Access to Chromosome Analysis, for Congenital Disorders, Blood is restricted.