• Cholesterol, Serum/Plasma
  • HLA-B75 (HLA-B*15:02) Genotyping for Carbamazepine Hypersensitivity
  • Aquaporin-4 (AQP4) Antibody, IgG, Cell-Binding-IFA Assay, Serum
  • Cholesterol, Body Fluid
  • Sodium, Serum
  • Chromosome Analysis, Products of Conception, or Stillbirth
  • B-Type Natriuretic Peptide (BNP) or Pro B-Type Natriuretic Peptide (Pro BNP)
  • West Nile Virus (WNV) Molecular Detection, Real-time PCR
  • Legius Syndrome (SPRED1) Sequencing
  • Wolf-Hirschhorn Syndrome, 4p16.3 Deletion
  • LDS
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  • /Medical Tests
  • /TGFB2 Gene Mutation Analysis
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  • Interpretation
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  • Methodology
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  • CPT
  • ICD10
  • Additional ICD10
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  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

TGFB2 Gene Mutation Analysis
Medical Test

Specimen Collection
Access to TGFB2 Gene Mutation Analysis is restricted.