Williams Syndrome, 7q11.23 Deletion, FISH, Tissue
Immunoglobulin M (IgM), Serum
EsoGuard Methylation Assay for Barrett’s Esophagus
Mycoplasma pneumoniae, Culture
Estrogen/Progesterone Receptor, IHC
HLA C Genotype
Lamotrigine, Urine
JAK2 (V617F) Gene Mutation Analysis
PML-RARA (Promyelocytic Leukemia/Retinoic Acid Receptor Alpha) Translocation, t(15;17) Analysis
Diabetic nephropathy
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
ICD10
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Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS
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