References
- Wilkins-Haug L, Hill LD, Schmidt L, et al. Genetics in obstetricians’ offices: a survey study. Obstet Gynecol 1999;93:642–7
- Bell CJ, Dinwiddie DL, Miller NA, et al. Carrier testing for severe childhood recessive diseases by next-generation sequencing. Sci Transl Med 2011;3:65ra4
- McGowan ML, Fishman JR, Settersten RA Jr, et al. Gatekeepers or intermediaries? The role of clinicians in commercial genomic testing. PLoS One 2014;9:e108484
- Lubin IM, Caggana M, Constantin C, et al. Ordering molecular genetic tests and reporting results: practices in laboratory and clinical settings. J Mol Diagn 2008;10:459–68
- American College of Obstetricians and Gynecologists Committee on Genetics. ACOG Committee Opinion No. 469: carrier screening for fragile X syndrome. Obstet Gynecol 2010;116:1008–10
- ACOG Committee on Genetics. ACOG committee opinion No. 432: spinal muscular atrophy. Obstet Gynecol 2009;113:1194–6
- American College of Obstetricians and Gynecologists Committee on Genetics. ACOG Committee Opinion No. 486: Update on carrier screening for cystic fibrosis. Obstet Gynecol 2011;117:1028–31
- Sherman S, Pletcher BA, Driscoll DA. Fragile X syndrome: diagnostic and carrier testing. Genet Med 2005;7:584–7
- Wilkins-Haug L, Hill LD, Power ML, et al. Gynecologists' training, knowledge, and experiences in genetics: a survey. Obstet Gynecol 2000;95:421–4
- Wilkins-Haug L, Erickson K, Hill L, et al. Obstetrician-gynecologists' opinions and attitudes on the role of genetics in women's health. J Women's Health Gend Based Med 2000;9:873–9
- Powell KP, Hasegawa L, McWalter K. Expanding roles: a survey of public health genetic counselors. J Genet Couns 2010;19:593–605