BDX-XL2, EarlyCDT®-Lung, Blood Test for Early Detection of Lung Cancer
Osmolality, Serum
MLYCD Gene Mutation Analysis, Blood
Cytochrome P450 3A4 (CYP3A4) Genotyping
Adenovirus DNA, Real-Time PCR, Quantitative
Cohen Syndrome Mutation Genetic Analysis
Leukotriene E4, Urine
Hemosiderin Stain, Urine
Calcium Channel Voltage-dependent L Type alpha 1S Subunit (CACNA1S) Gene Mutation Analysis
Bone Marrow Aspiration
LDS
Sign up
Log in
LDS
/
Medical Tests
/
Carnitine Palmitoyltransferase II Deficiency, 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
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
Medical Test
Diseases (1)
Access to
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
is restricted.
Sign up now