Prenatal SOX9 Gene Sequencing and Del/Dup

Forms and Documents

Test Details

SOX9
  • Full sequencing and deletion/duplication testing for fetuses with ultrasound findings suggestive of CD
  • Mutation-specific testing for fetuses with a family history of a known SOX9 mutation
  • Exon Array CGH
  • Next-Gen Sequencing

Ordering

3383
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. Mansour et al., (1995) J Med Genet 32:415-420
  2. Mansour et al., (2002) J Med Genet 39:597-602
  3. Wagner et al., (Cell) 79:1111-1120
  4. Cameron et al., (1996) Hum Mol Genet 5(10):1625-1630
  5. Smyk et al., (2007) Am J Med Genet 143A(8):866-870
  6. Pop et al., (2004) J Med Genet 41:e47
  7. Meyer et al., (1997) Hum Mol Genet 6(1):91-98
  8. Pop et al. (2005) Hum Genet 117:43-53
  9. Huang et al., (1999) Am J Med Genet 87:349-353
  10. Refai et al., (2010) Am J Med Genet A 152A:422-426
  11. Moog et al., (2001) Am J Med Genet 104:239-245