Bordetella pertussis Culture
Biopsy, Blood Vessel
Primary Hyperoxaluria Gene Mutation Panel
G6PC (Glucose-6-phosphatase, Catalytic Subunit), Glycogen Storage Disease Type 1 (von Gierke Disease) Gene Mutation Analysis
CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
Products of Conception (POC) Aneuploidy Detection, FISH, Tissue
Lupus nephritis
Thyroid Stimulating Immunoglobulin (TSI)
Renin Activity
Transthyretin (TTR) Gene Mutation Analysis
LDS
Sign up
Log in
LDS
/
Medical Tests
/
Comprehensive Mitochondrial Disorders Gene Analysis Panel, NGS (Genomic Unity®)
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
Comprehensive Mitochondrial Disorders Gene Analysis Panel, NGS (Genomic Unity®)
Medical Test
Overview
Access to
Comprehensive Mitochondrial Disorders Gene Analysis Panel, NGS (Genomic Unity®)
is restricted.
Sign up now