Prenatal (Obstetrics) Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
X and Y Aneuploidy Detection, FISH
Phospholamban (PLN) Gene Mutation Analysis
Neuron Specific Enolase (NSE), CSF
Streptococcus pneumoniae Antigen, Urine
Acetylcholinesterase (AChE), Amniotic Fluid
Mumps Virus Antibody, IgG, IgM
Kell K/k Antigen (KEL) Genotyping
Amyotrophic Lateral Sclerosis Gene Mutation Panel, NGS
Clonidine (Catapres), Urine
LDS
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Primary Hyperoxaluria Gene Mutation Panel
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Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
Primary Hyperoxaluria Gene Mutation Panel
Medical Test
Additional Testing
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Primary Hyperoxaluria Gene Mutation Panel
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