Williams Syndrome, 7q11.23 Deletion, FISH, CV
Biopsy, Salivary Gland
Alpha Fetoprotein (AFP), Body Fluid
Bladder Cancer Diagnosis by FISH (UroVysion)
Glucose-6-Phosphate Dehydrogenase (G6PD)
Glomerular Filtration Rate, Estimated (eGFR)
PPP2R2B (Protein Phosphatase 2 Regulatory Subunit Beta) Gene Mutation Analysis
Myelin Oligodendrocyte Glycoprotein (MOG), Antibody, Serum
17-Hydroxyprogesterone, Amniotic fluid
N-Telopeptide, Cross-Linked
LDS
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Lynch Syndrome Multi Gene Panel (MLH1, MSH2, MSH6, PMS2 and EPCAM), Genomic Unity®
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
Lynch Syndrome Multi Gene Panel (MLH1, MSH2, MSH6, PMS2 and EPCAM), Genomic Unity®
Medical Test
Clinical Utility
Access to
Lynch Syndrome Multi Gene Panel (MLH1, MSH2, MSH6, PMS2 and EPCAM), Genomic Unity®
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