Fanconi Anemia Type C Gene Mutation Analysis
Mercury, Blood
CD4 Lymphocyte Count
Ganglioside (GM1) Antibody, IgG and IgM
Sarcoma Gene Mutation, Fusion and Rearrangement Panel, NGS
Desipramine, Serum
Ulcerative colitis
Chromosome Analysis, Interphase, FISH
Acid Phosphatase, Total, Serum
Cardiac Ion Channelopathies Multi-Gene Panel, NGS

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/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

Reference Ranges

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