• Tissue Transglutaminase (tTG) Antibody, IgA
  • Protoporphyrins, Fractionation, Whole Blood
  • Beta-Galactosidase, Fibroblasts
  • Beta-2 Microglobulin, Urine
  • Herpes Simplex Virus (HSV) 1 and 2 by PCR
  • Phospholipase C Gamma 2 (PLCG2) Gene Mutation Analysis
  • Legionella Antigen, Urine
  • Chlamydia trachomatis and Neisseria gonorrhoeae NA, Urine
  • Measles (Rubeola) Virus Culture, CSF
  • Norovirus, EIA, Stool
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  • /Chromosome Analysis, for Congenital Disorders, Blood
  • All
  • 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

Chromosome Analysis, for Congenital Disorders, Blood
Medical Test

Specimen Collection
Access to Chromosome Analysis, for Congenital Disorders, Blood is restricted.