Amphetamines/Sympathomimetic Amines, Urine
Beta-2 Microglobulin, Serum
Noonan Spectrum Disorders Gene Mutation Panel, NGS
Williams Syndrome, 7q11.23 Deletion, FISH, Amniotic Fluid
Alkaline Phosphatase Isoenzymes
Legius Syndrome (SPRED1) Sequencing
Anemia Panel
Osmolality, Body Fluid
SMAD4 Germline Mutation Analysis
Thyroid hormone uptake (T Uptake)
LDS
Sign up
Log in
LDS
/
Medical Tests
/
PHOX2B 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
PHOX2B gene mutation analysis
Medical Test
References
Access to
PHOX2B gene mutation analysis
is restricted.
Sign up now