Complete Urinalysis
X-linked Intellectual Disability Gene Mutation Panel, NGS
FoundationOne®CDx (F1CDx) and FoundationOne® Liquid CDx
Multiple Sclerosis Panel
Cytochrome P450 3A7 (CYP3A7) Genotyping
Glucose, Random, Urine
T-Cell Receptor Gene Rearrangement, Flow Cytometry, Bone Marrow
Jo 1 Antibody, IgG
Whole Exome Sequence Analysis, NGS
Hepatitis C Virus (HCV) Antibody
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Peutz-Jeghers Syndrome (STK11) Gene Mutation Analysis
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
Peutz-Jeghers Syndrome (STK11) Gene Mutation Analysis
Medical Test
CPT
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Peutz-Jeghers Syndrome (STK11) Gene Mutation Analysis
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