1p36.3 Microdeletion Syndrome, FISH
Genetic Testing for Severe Inherited Diseases, NGS
Ethanol (Alcohol), Urine
Norovirus, EIA, Stool
Fentanyl, Urine
Estrone, Serum
CaM Kinase II (CaMKII, Calcium-dependent Calmodulin Protein Kinase II) Activation
Bilirubin Total, Serum
Epstein-Barr Virus (EBV), Real-Time PCR
Influenza Virus Type A, B and Respiratory Syncytial Virus (RSV), PCR
LDS
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Chromosome Analysis, Lymphoid Tissue
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
Chromosome Analysis, Lymphoid Tissue
Medical Test
Interpretation
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Chromosome Analysis, Lymphoid Tissue
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