Prenatal SRD5A2 Gene Sequencing

Forms and Documents

Test Details

SRD5A2
  • Full gene sequencing for fetuses with prenatal ultrasound findings suggestive of 46,XY disorder of sex development
  • Mutation-specific testing for fetuses with a family history of known SRD5A2 mutations
  • Capillary Sequencing

Ordering

702
2-3 weeks
20 mL Amniotic Fluid
20 mg CVS|2 T25 flasks of cultured amniocytes|2 T25 flasks of cultured chorionic villi|3 Ug DNA Concentration

Billing

81479x1, 81265x1
No
Yes
* For price inquiries please email zebras@genedx.com

References

  1. Maimoun et al., (2011) J Clin Endocrinol Metab 96:296-307.
  2. Thigpen et al., (1992) J Clin Invest 90:799-809.
  3. Hackel et al., (2005) J Mol Med 83:569-576.
  4. Vilchis et al., (2010) J Androl 31:358-364.
  5. Sasaki et al., (2003) J Clin Endocrinol Metab 88:3431-3436.
  6. Wang et al., (2004) Eur J Hum Genet 12:706-712.
  7. Andersson et al., (1991) Nature 354:159-161.
  8. Mazen et al., (2003) Clin Endocrinol 58:627-631.
  9. Makridakis et al., (1997) Cancer Res 57:1020-1022.