Thyroid Cancer Gene Panel from FNA (Afirma®, ThyGenX/ThyraMIR, ThyroSeq v2, RosettaGX Reveal)
Cytochrome P450 3A7 (CYP3A7) Genotyping
Hypertrophic Cardiomyopathy Gene Mutation Panel, NGS
TGFBI Gene Mutation Analysis
Albumin, 24 Hour, Urine
Vitamin B2 (Riboflavin)
Congenital adrenal hyperplasia
Coxsackie A Virus Antibodies, CSF
Bilirubin Total, Amniotic Fluid
B-cell Activating Factor Receptor (BAFF-R) Gene Mutation Analysis
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Chromosome Analysis, Routine, Blood
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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
Chromosome Analysis, Routine, Blood
Medical Test
LOINC
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Chromosome Analysis, Routine, Blood
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