Williams Syndrome, 7q11.23 Deletion, FISH, Tissue
Vascular Endothelial Growth Factor (VEGF)
Gentamicin, Peak, Serum
Human Platelet Antigen 1 (HPA-1) Genotyping
Pheochromocytoma
MSH2 Gene Mutation Analysis (Known Mutations, Duplication/Deletion/Sequencing)
Hydroxyzine, Serum
MLH1 Hypermethylation (Promoter Methylation) Analysis, Tissue
T Cell Lymphoma, FISH, Bone Marrow
RET Gene Rearrangements by FISH
LDS
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NHP2 Gene Mutation Analysis
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
NHP2 Gene Mutation Analysis
Medical Test
CPT
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NHP2 Gene Mutation Analysis
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