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Prenatal TP73L (TP63) Gene Sequencing

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
TP63 (TP73L)
Disorders:
Clinical Utility:
  • Full gene sequencing for fetuses with prenatal ultrasound findings suggestive of EEC or related syndromes.
  • Mutation-specific testing for fetuses with a family history of a known TP73L (TP63) mutation
Lab Method:
Capillary Sequencing

ORDERING

Test Code:
407
Turnaround Time:
2-3 weeks
Preferred Specimen:
20 mL Amniotic Fluid
Alternative Specimen:
20 mg CVS, 2 T25 flasks of cultured amniocytes, 2 T25 flasks of cultured chorionic villi

BILLING

CPT Codes:
81479x1, 81265x1, 88235x1
New York Approved:
No
ABN Required:
Yes
Billing Information:
View Prenatal Billing Policy
ICD Codes:
  • 655.23: Hereditary disease in family possibly affecting fetus
  • 655.83: Other known or suspected fetal abnormality, not elsewhere classified
* For price inquiries please email zebras@genedx.com

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