Haptoglobin Genotyping
Spinobulbar Muscular Atrophy (Kennedy Disease), Androgen Receptor Gene Mutation Analysis
Blastomyces Antigen, Quantitative, Serum
Carbamazepine, Free and Total, Serum
Chlamydia pneumoniae, Culture
Heavy Metals, Blood
Cri-du-chat Syndrome, 5p15.2 Deletion, FISH
Alpha Fetoprotein (AFP), Amniotic Fluid
AGXT Gene Mutation Analysis
Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS

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LDS
/Medical Tests
/Chromosome Breakage Study, Chorionic Villi

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 Breakage Study, Chorionic Villi
Medical Test

Reference Ranges

Access to Chromosome Breakage Study, Chorionic Villi is restricted.

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