Genetic Testing Company | The DNA Diagnostic Experts | GeneDx

In observance of the holidays, GeneDx will be closed for business on Thursday, December 25, 2014 and on Thursday, January 1, 2015. We will be unable to receive and process specimens. FedEx and UPS will also not be in operation. Except for the aforementioned dates, GeneDx will operate on our normal schedule (Monday-Saturday), including December 24th and December 31st.  If you have any questions or inquiries, please call us at 301-519-2100 or email us at zebras@genedx.com.

VSX2 (CHX10) Gene Sequencing

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
VSX2 (CHX10)
Disorders:
Clinical Utility:
  • Confirmation of a clinical diagnosis
  • Prenatal diagnosis
Lab Method:
Capillary Sequencing

ORDERING

Test Code:
344
Turnaround Time:
6-8 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:
  • 743.11: Simple microphthalmos
  • 743.9: Unspecified anomaly of eye
  • 743.1: Microphthalmos, unspecified
* For price inquiries please email zebras@genedx.com

REFERENCES

  1. Schneider et al. (2009) Am J Med Genet 149A(12)2706-2715
  2. Bakrania et al. (2007) Br J Ophthalmol 91:1471-17476
  3. E. Ferda Percin et al., (2000) Nat Genet 25(4):397-401
  4. Aijaz S et al (2004) Invest Ophthalmol Vis Sci. 45(11):3871-6
  5. Ragge NK et al., (2005) Am J Hum Genet. 276(6):1008-22
  6. Bar-Yosef U et al., (2004) Hum Genet 115: 302–309
  7. Ragge NK et al., (2007) Eye 21(10):1290-300
  8. Wyatt A et al., (2008) Hum Mutat. (2008) 29(11):E278-83
  9. Elliott J et al., (1993) 30(3):251-2
  10. Bennett CP (1991) J Med Genet 1991;28:280-1
  11. Gallardo, ME et al., (2004) Am J Med Genet 129A:92
  12. Fantes, J et al (2003) Nature Genetics 33:462
  13. Gallardo ME et al., (1999) Genomic 61:82
  14. Hagstrom SA et al. (2005) Am J Med Genet (2005) 138(2):95
  15. Forrester and Merz (2006) Birth Defects Res A Clin Mol Terato 76:187-192
  16. Williamson, KA et al. (2006) Hum Mol Genet 15(9):1413

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