Apolipoprotein B, Serum
Cephalosporin IgE
PML-RARA (Promyelocytic Leukemia/Retinoic Acid Receptor Alpha) Translocation, t(15;17) Analysis
Psychosis, unspecified
Factor IX Gene Gene Mutation Analysis
Specific Gravity, Body Fluid
CaM Kinase II (CaMKII, Calcium-dependent Calmodulin Protein Kinase II) Activation
Meprobamate, Urine
4q25 Atrial Fibrillation Risk Genotype Test
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
LDS
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1p36.3 Microdeletion Syndrome, FISH
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
1p36.3 Microdeletion Syndrome, FISH
Medical Test
Methodology
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1p36.3 Microdeletion Syndrome, FISH
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