• Acetaminophen, Serum
  • Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum
  • Bone Morphogenetic Protein Receptor Type 1A (BMPR1A) Gene Mutation Analysis
  • Triglycerides, Serum
  • Fine Needle Aspiration, Breast
  • Vitamin B6 (Pyridoxal Phosphate)
  • Histoplasma capsulatum Antigen, CSF
  • ADAMTS2 Gene Mutation Analysis
  • Survival of Motor Neuron 1 (SMN1) Mutation Analysis
  • Brain-derived Neurotrophic Factor (BDNF) Genotyping
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  • /FBN1 (Fibrillin-1) Genetic Mutation Analysis
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  • CPT
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  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References

FBN1 (Fibrillin-1) Genetic Mutation Analysis
Medical Test

References
Access to FBN1 (Fibrillin-1) Genetic Mutation Analysis is restricted.