Pernicious anemia
Wolf-Hirschhorn Syndrome, 4p16.3 Deletion
Oxymorphone, Urine
Phospholipid (Cardiolipin) Antibody, IgM
Immunophenotypic Analysis of Tissues by Flow Cytometry
Asymmetric Dimethylarginine, Plasma
Bone Morphogenetic Protein Receptor Type II (BMPR2) Gene Mutation Analysis
Pheniramine, Urine
Maternal Serum Screen (Quad Screen), Second Trimester
Vitamin A deficiency
LDS
Sign up
Log in
LDS
/
Medical Tests
/
MYL3 Gene Mutation Analysis
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
MYL3 Gene Mutation Analysis
Medical Test
Methodology
Access to
MYL3 Gene Mutation Analysis
is restricted.
Sign up now