Genetic Testing Company | The DNA Diagnostic Experts | GeneDx

In observance of the holiday, GeneDx will be closed for business on Thursday, November 27, 2014, and will be unable to receive and process specimens. FedEx and UPS will also not operate. We will accept specimens on Friday, November 28, and  will resume our normal work schedule on Saturday, November 29, 2014.  If you have any questions or inquiries, please call us at 301-519-2100 or email us at zebras@genedx.com.

ZRS Del/Dup Analysis (Intron 5 of LMBR1 Gene)

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
LMBR1
Disorders:
Clinical Utility:
  • Confirmation of a clinical diagnosis
  • Differentiation from other causes of syndromic and isolated limb abnormalities
  • Prenatal diagnosis in families with a known mutation
Lab Method:
Exon Array CGH

ORDERING

Test Code:
906
Turnaround Time:
3-4 weeks
Preferred Specimen:
2-5 mL Blood - Lavender Top Tube

BILLING

CPT Codes:
84311x1, 88271x10, 88291x1
New York Approved:
Yes
ABN Required:
Yes
Billing Information:
View Billing Policy
ICD Codes:
  • 755.1: Syndactyly Symphalangy Webbing of digits
  • 755.00: Polydactyly, unspecified digits Supernumerary digits
  • 755: Other congenital anomalies of limbs Excludes: those deformities classifiable to 754.0-754.8
  • 759.7: Multiple congenital anomalies, so described Congenital: anomaly, multiple NOS deformity, multiple NOS
* For price inquiries please email zebras@genedx.com

REFERENCES

  1. Wu et al., (2009) Am J Med Genet Part A 149A:816-818.
  2. Wieczorek et al., (2010) Hum Mutat 31(1):81-89.
  3. Sun et al., (2008) J Med Genet 45:589-595.
  4. Semerci et al., (2009) Clin Genet 76:85-90.
  5. Klopocki et al., (2008) J Med Genet 45:370-375.
  6. Gurnett et al., (2007) Am J Med Genet Part A 143A:27-32.
  7. Furniss et al., (2009) J Med Genet 46:730-735.
  8. Furniss et al., (2008) Hum Mol Genet 17(16):2417-2423.

Back To Top