Vitamin B6 (Pyridoxal Phosphate)
Immunoglobulin M (IgM), Serum
Williams Syndrome, 7q11.23 Deletion, FISH, Tissue
HIV Co-Receptor Tropism (Trofile) Assay
Mycoplasma pneumoniae, Culture
Estrogen/Progesterone Receptor, IHC
Splicing Factor 3b Subunit B1 (SF3B1) Gene Mutation Analysis
Glycogen storage disease type I (von Gierke disease)
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
Lamotrigine, Urine

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LDS
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/Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS

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

Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS
Medical Test

Access to Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS is restricted.