Fibrinogen Antigen
Whole Exome Sequence Analysis, NGS
HLA A Genotype
Pheniramine, Urine
Glucose, Random, Urine
Nickel, Serum
HER2/neu (ERBB2), IHC, Semi Quantitative, Automated
Porphobilinogen, Quantitative, Random, Urine
Acute coronary syndrome
Cystatin B (CSTB) Gene Mutation Analysis

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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

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