Specific References
American College of Obstetricians and Gynecologists Committee on Genetics. The use of chromosomal microarray analysis in prenatal diagnosis. Obstet Gynecol. 2009;122:1374–1377.
American College of Obstetricians and Gynecologists Committee on Genetics. Noninvasive prenatal testing for fetal aneuploidy. Obstet Gynecol. 2012;120:1532–1534.
Bianchi D. From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges. Nat Med. 2012;18:1041–1051.
Bianchi DW, Parker RL, Wentworth J, et al. DNA sequencing versus standard prenatal aneuploidy screening. N Engl J Med. 2014;370(9):799–808.
Bodurtha J, Strauss JF. Genomics and perinatal care. N Engl J Med. 2012;366:64–73.
Chitayat D, Langlois S, Wilson RD, et al. Prenatal screening for fetal aneuploidy in singleton pregnancies. J Obstet Gynaecol Can. 2011;33:736–750.
Dugoff L. Application of genomic technology in prenatal diagnosis. N Engl J Med. 2012;367:2249–2251.
Duncan A, Langlois S, SOGC Genetics Committee, et al. Use of array genomic hybridization technology in prenatal diagnosis in Canada. J Obstet Gynaecol Can. 2011;33:1256–1259.
Fan HC, Gu W, Wang J, et al. Non-invasive prenatal measurement of the fetal genome. Nature. 2012;487:320–324.
Gregg A, Gross SJ, Best RG, et al. ACMG statement on noninvasive prenatal screening for fetal aneuploidy. Genet Med. 2013;15:395–398.
Malone FD, Canick JA, Ball RH, et al. First-trimester and second-trimester screening, or both, for Down’s Syndrome. N Engl J Med. 2005;353:2001–2011.
McArthur SJ, Leigh D, Marshall JT, et al. Blastocyst trophectoderm biopsy and preimplantation genetic diagnosis for familial monogenic disorders and chromosomal translocations. Prenat Diagn. 2008;28:434–442.
Norwitz ER, Levy B. Noninvasive prenatal testing: the future is now. Rev Obstet Gynecol. 2013;6:48–62.
Talkowski ME, Ordulu Z, Pillalamarri V, et al. Clinical diagnosis by whole-genome sequencing of a prenatal sample. N Engl J Med. 2012;367:2226–2232.
Wapner RJ, Martin CL, Levy B, et al. Chromosomal microarray versus karyotyping for prenatal diagnosis. N Engl J Med. 2012;367:2175–2184.
Yurkiewicz IR, Korf BR, Lehmann LS. Prenatal whole-genome sequencing – is the quest to know a fetus’ future ethical? N Engl J Med. 2014;370:195–197.