DMPK Gene Analysis for Myotonic Dystrophy Type I (DM1)
Williams Syndrome, 7q11.23 Deletion, FISH, Amniotic Fluid
Uniparental Disomy, FISH, Amniotic Fluid
von Willebrand Disease 2N (Subtype Normandy), Genotyping
Coagulation Factor XI Activity Assay, Plasma
Hepatitis B Surface Antibody, Quantitative
Biopsy, Pericardial
Respiratory Pathogen Panel Including SARS-CoV-2, Molecular
Aldosterone, 24 Hour, Urine
Thyroid Stimulating Immunoglobulin (TSI)
LDS
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F2-Isoprostanes, Urine
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CPT
LOINC
ICD10
Additional ICD10
All
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CPT
LOINC
ICD10
Additional ICD10
F2-Isoprostanes, Urine
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