Smith-Magenis/Potocki-Lupski Syndromes, 17p11.2 Deletion/Duplication, FISH
UBE3A Gene Mutation Analysis, Angelman Syndrome, Blood
Prenatal RhD NIPT Cell-free DNA Screening (UNITY Fetal Antigen™, Fetal RhD NIPT Panorama™)
Carcinoembryonic Antigen (CEA), Peritoneal Fluid
Chikungunya Virus RNA, Real-Time PCR, Qualitative
Red Blood Cell Antigen Genotyping (Immucor PreciseType, BLOODchip® ID CORE XT™, Prenatal Detect RhD)
Homocysteine, Urine
Eurofins TRAC® Test for Monitoring Kidney Transplant Health
Inducible Costimulator (ICOS) Gene mutation analysis
Dopamine receptor 1 (DRD1) Genotyping
LDS
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Neurotrophic Receptor Tyrosine Kinase 3 (NTRK3) Gene Mutation Analysis (Translocation)
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
Neurotrophic Receptor Tyrosine Kinase 3 (NTRK3) Gene Mutation Analysis (Translocation)
Medical Test
Additional Testing
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Neurotrophic Receptor Tyrosine Kinase 3 (NTRK3) Gene Mutation Analysis (Translocation)
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