ASXL1 Gene Mutation Analysis
Salla disease
Catecholamine Fractionation, Free, 24 Hour, Urine
Protein, Total, 24 Hour, Urine
Lipoprotein Associated Phospholipase A2 Activity
Adenovirus DNA, Real-Time PCR, Quantitative
Oncology Pharmacogenetics (PGx) Gene Variation Panel
Coagulation Factor VII Inhibitor Screen, Plasma
Androgen insensitivity syndrome
ATM/C11orf65 Gene Variation

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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.