Cardio Pharmacogenetics (PGx) Gene Variation Panel
Apolipoprotein B (APOB) Mutation Detection
22q11.2 Deletion/Duplication, FISH
Prolyl Hydroxylase Domain-2 (PHD2/EGLN1) Gene Mutation Analysis
Carbamazepine, Free, Serum
HLA typing; A, B, or C, Single or Multiple Antigens
Benzene Quantitative, Whole Blood
Hemangioma of liver
Prostate Health Index (phi score, 4Kscore®), Serum
CHIC2, 4q12 Deletion (FIP1L1 and PDGFRA Fusion), FISH, Blood
LDS
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PTPN11 Gene Mutation Analysis for Noonan Syndrome
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
PTPN11 Gene Mutation Analysis for Noonan Syndrome
Medical Test
Diseases (2)
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PTPN11 Gene Mutation Analysis for Noonan Syndrome
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