• Fetal Fibronectin (fFN)
  • Acetylcholinesterase (AChE), Amniotic Fluid
  • Phosphorylated Tau 181 (pTau-181), Plasma
  • Cholesterol, Serum/Plasma
  • HLA-B75 (HLA-B*15:02) Genotyping for Carbamazepine Hypersensitivity
  • 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)
  • Wolf-Hirschhorn Syndrome, 4p16.3 Deletion
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /TGFB2 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

TGFB2 Gene Mutation Analysis
Medical Test

Specimen Collection
Access to TGFB2 Gene Mutation Analysis is restricted.