ASXL1 Gene Mutation Analysis
Compatibility Tests (Crossmatch), ABO, Rh Typing
Vitamin B12 (Cyanocobalamin)
Poly A Binding Protein Nuclear 1Gene (PABPN1) Mutation Analysis
HBB (Hemoglobin, Subunit Beta) Gene Mutation Analysis
Catecholamine Fractionation, Free, 24 Hour, Urine
Adenosine Deaminase, CSF
Protein, Total, 24 Hour, Urine
Vascular Endothelial Growth Factor (VEGF)
Gene Expression Test for Monitoring Heart Transplant Rejection (AlloMap, MMDx Heart, myTAIHEART)

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/Chromosome Analysis, for Congenital Disorders, Blood

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

Chromosome Analysis, for Congenital Disorders, Blood
Medical Test

Reference Ranges

Access to Chromosome Analysis, for Congenital Disorders, Blood is restricted.