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)
Histoplasma Antigen, CSF
LDS
Sign up
Log in
LDS
/
Medical Tests
/
DMPK Gene Analysis for Myotonic Dystrophy Type I (DM1)
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
DMPK Gene Analysis for Myotonic Dystrophy Type I (DM1)
Medical Test
Methodology
Access to
DMPK Gene Analysis for Myotonic Dystrophy Type I (DM1)
is restricted.
Sign up now
Loading...