MI Cancer Seek® Companion Diagnostic Molecular Profiling Test for Solid Tumors
Paroxysmal Nocturnal Hemoglobinuria (PNH) (CD55, CD59), Flow, Blood
PPOX Gene Mutation Analysis, Blood
Spinocerebellar Ataxia, Ataxin 8 (ATXN8OS) Gene Mutation Analysis
Malaria/Babesia Blood Smear
Thyroglobulin, Fine Needle Aspiration (FNA)
Prolactin
CEBPA (CCAAT enhancer binding protein alpha) Gene Mutation Analysis
Propofol (Diprivan), Serum
Phenylephrine, Urine or Serum
LDS
Sign up
Log in
LDS
/
Medical Tests
/
Spinocerebellar Ataxia Type 1 (ATXN1) Gene Mutation Analysis
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
Spinocerebellar Ataxia Type 1 (ATXN1) Gene Mutation Analysis
Medical Test
Diseases (3)
Access to
Spinocerebellar Ataxia Type 1 (ATXN1) Gene Mutation Analysis
is restricted.
Sign up now
Loading...