Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Gene Mutation Analysis
FLT3 (FMS-related Tyrosine Kinase 3) Mutation Analysis, Blood
Homovanillic Acid (HVA), Random, Urine
Neurofibromatosis Type 1 (NF1) Gene Mutation Analysis
Hepatitis C Virus (HCV) Genotyping
MYH7 Gene Mutation Analysis
Chromogranin A
Selenium, Serum
Adiponectin
Inhibin A

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/Wolf-Hirschhorn Syndrome, 4p16.3 Deletion

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

Wolf-Hirschhorn Syndrome, 4p16.3 Deletion
Medical Test

Reference Ranges

Access to Wolf-Hirschhorn Syndrome, 4p16.3 Deletion is restricted.

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