• Cervical intraepithelial neoplasia
  • Chlorpheniramine, Urine
  • Bartonella, Molecular Detection, PCR
  • Polycystic kidney disease
  • Acute conjunctivitis
  • Neurotrophic Receptor Tyrosine Kinase 2 (NTRK2) Gene Mutation Analysis (Translocation)
  • No Specific Laboratory Tests
  • Polyoma BK virus infections
  • Triglycerides, Serum
  • 1p36 deletion (monosomy) syndrome
  • LDS
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  • /Kallmann Syndrome, Xp22.3 Deletion, FISH
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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

Kallmann Syndrome, Xp22.3 Deletion, FISH
Medical Test

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Access to Kallmann Syndrome, Xp22.3 Deletion, FISH is restricted.
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