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FOXC1 Gene Sequencing

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
FOXC1
Disorders:
Clinical Utility:
  • Confirmation of a clinical diagnosis
  • Recurrence risk calculation
  • Prenatal diagnosis in families with known mutation
Lab Method:
Capillary Sequencing

ORDERING

Test Code:
1342
Turnaround Time:
4-6 weeks
Preferred Specimen:
2-5 mL Blood - Lavender Top Tube

BILLING

CPT Codes:
81479x1
New York Approved:
No
ABN Required:
Yes
Billing Information:
View Billing Policy
ICD Codes:
  • 743.9: Specified congenital anomalies of anterior chamber, chamber angle, and related structures.
  • 743.9: Unspecified anomaly of eye
* For price inquiries please email zebras@genedx.com

REFERENCES

  1. Mears et al. (1998) Am J Hum Genet 63:1316-1318
  2. Nishimura et al. (2001) American Journal of Human Genetics 68(2):364-372
  3. Priston et al. (2001) Human Molecular Genetics 10(16):1631-1638
  4. Perveen et al. (2000) Invest Ophthalmol Vis Sci.41(9):2456-2460
  5. Lines et al. (2004) Invest Ophthalmol Vis Sci.Science 45(3):828-833
  6. Hjalt et al. (2005) Expert Reviews in Molecular Medicine 7(25)1-15
  7. Semina et al. (1996) Nat Genet 14:392-399

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