Inhibin A and B, Tumor Marker
Chromosome Breakage Study, Bone Marrow
Branched-chain-ketoacid dehydrogenase (BCKDH) Gene Mutation Analysis
Platelet Antibodies, Serum
Autopsy
UBE3A Gene Mutation Analysis, Angelman Syndrome, Blood
Melanocytic nevus
CEBPA (CCAAT enhancer binding protein alpha) Gene Mutation Analysis
Collagen Type II, Antibody
Osmolality, Urine

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/Medical Tests
/CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)

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

CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
Medical Test

Turnaround Time

Access to CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2) is restricted.