1p36 deletion (monosomy) syndrome
Inflammatory bowel disease
Immunoglobulin G (IgG)
Fragile X syndrome
Prealbumin (Transthyretin)
Primary fibromyalgia syndrome
Chronic gastritis
Hypobetalipoproteinemia
Myotonic dystrophy
Portal vein thrombosis
LDS
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MEK1 Mutation Analysis, Melanoma
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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
MEK1 Mutation Analysis, Melanoma
Medical Test
Reference Ranges
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MEK1 Mutation Analysis, Melanoma
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