• Fibroblast Growth Factor Receptor 1 (FGFR1), 8p11.2 Rearrangement, FISH, Blood
  • Platelet Antibodies, Serum
  • 15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
  • Hepatitis B Core Antibody, IgG
  • Leukemia/Lymphoma Immunophenotyping by Flow Cytometry, Blood
  • Insulin-Like Growth Factor Binding Protein 3 (IGFBP-3)
  • Salmonella Antibodies
  • NRAS (Neuroblastoma RAS Viral Oncogene Homolog) Gene Mutation Analysis
  • Culture, Body Fluid
  • Adrenoceptor Alpha 2A Polymorphism (ADRA2A)
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  • /Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
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  • 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

Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
Medical Test

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