UBE3A Gene Mutation Analysis, Angelman Syndrome, Blood
Carcinoembryonic Antigen (CEA), Peritoneal Fluid
Prenatal RhD NIPT Cell-free DNA Screening (UNITY Fetal Antigen™, Fetal RhD NIPT Panorama™)
Red Blood Cell Antigen Genotyping (Immucor PreciseType, BLOODchip® ID CORE XT™, Prenatal Detect RhD)
Eurofins TRAC® Test for Monitoring Kidney Transplant Health
Chikungunya Virus RNA, Real-Time PCR, Qualitative
Homocysteine, Urine
Chromosome Analysis, Sister Chromatid Exchange (SCE) for Bloom Syndrome, Blood
Dopamine receptor 1 (DRD1) Genotyping
BCR-ABL, Translocation, FISH, Blood
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Smith-Magenis/Potocki-Lupski Syndromes, 17p11.2 Deletion/Duplication, FISH
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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
Smith-Magenis/Potocki-Lupski Syndromes, 17p11.2 Deletion/Duplication, FISH
Medical Test
Reference Ranges
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Smith-Magenis/Potocki-Lupski Syndromes, 17p11.2 Deletion/Duplication, FISH
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