UBE3A Gene Mutation Analysis, Angelman Syndrome, Blood
Prenatal RhD NIPT Cell-free DNA Screening (UNITY Fetal Antigen™, Fetal RhD NIPT Panorama™)
Smith-Magenis/Potocki-Lupski Syndromes, 17p11.2 Deletion/Duplication, FISH
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
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Smith-Magenis/Potocki-Lupski Syndromes, 17p11.2 Deletion/Duplication, 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
Smith-Magenis/Potocki-Lupski Syndromes, 17p11.2 Deletion/Duplication, FISH
Medical Test
Interpretation
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Smith-Magenis/Potocki-Lupski Syndromes, 17p11.2 Deletion/Duplication, FISH
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