1p36.3 Microdeletion Syndrome, FISH
Paroxysmal nocturnal hemoglobinuria
Immunoperoxidase Stain
Culture, Group B Streptococcus (GBS)
Heavy Metals, Blood
Pregnancy Test, Manual
Copper, Liver Tissue
Complement Component C1q
Imipramine, Serum
Kappa and Lambda Free Light Chains, Quantitative, Serum
LDS
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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
Additional Testing
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Peutz-Jeghers Syndrome (STK11) Gene Mutation Analysis
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