DNA Collection

Cheek Swab

Turn-around Time

7-10 business days

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References: 1. ACOG Committee Opinion Number 691, Carrier Screening for Genetic Conditions (2017). 2. ACOG Committee Opinion Number 486. Update on carrier screening for cystic fibrosis (2011). 3. ACOG Committee Opinion Number 442. Preconception and prenatal carrier screening for genetic disease in individuals of Eastern European Jewish descent. Obstet Gynecol. 2009;114(4):950-953. 4. ACOG Committee Opinion Number 318. Screening for Tay Sachs disease (2005). 5. ACOG Committee Opinion Number 469. Carrier screening for Fragile X syndrome (2010). 6. ACMG Policy Statement. Laboratory standards and guidelines for population based cystic fibrosis carrier screening (2001). 7. Watson MS, Cutting GR, Desnick RJ, et al. Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel [published corrections appear in Genet Med. 2004;6(6):548 and Genet Med. 2005;7(4):286]. Genet Med. 2004;6(5):387-391. 8. ACMG Practice Guideline. Carrier screening for Spinal Muscular Atrophy (2008). 9. ACMG Practice Guidelines. Carrier screening in individuals of Ashkenazi Jewish descent. Genet Med. 2008;10(1):54-56. 10. ACMG Practice Guidelines. Technical standards and guidelines for reproductive screening the AJ population (2008). 11. ACMG Practice Guidelines. Technical standards and guidelines for reproductive screening the AJ population (2008). 12. ACMG Practice Guideline. Fragile X syndrome: diagnostic and carrier testing (2005). 13. ACMG Practice Guideline. Preconception and prenatal testing of biologic fathers for carrier status (2006). 14. Wirth B. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA). Hum Mutat. 2000; 15(3):228-37. 15. Prior TW, Russman BS. Spinal Muscular Atrophy. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016. 2000 Feb 24 [updated 2013 Nov 14]. 16. Hendrickson BC, Donohoe C, Akmaev VR, et al. Differences in SMN1 allele frequencies among ethnic groups within North America. J Med Genet. 2009 Sep; 46(9):641-4.