［1］Edwards JH, Harnden DG, Cameron AH, Crosse VM, Wolff OH. A new trisomic syndrome［J］. Lancet, 1960, 1(7128): 787-790.
［2］Rasmussen SA, Wong L, Yang Q, May K, Friedman JM. Population-based analyses of mortality in trisomy 13 and trisomy 18［J］. Pediatrics, 2003, 111(4): 777-784.
［3］Won RH, Currier RJ, Lorey F, Towner DR. The timing of demise in fetuses with trisomy 21 and trisomy 18［J］. Prenat Diagn, 2005, 25(7): 608-611.
［4］Savva GM, Walker K, Morris JK. The maternal age-specific live birth prevalence of trisomies 13 and 18 compared to trisomy 21 (down syndrome)［J］. Prenat Diagn, 2010, 30(1):57-64.
［5］Schmidt L,Sobotka T, Bentzen JG, Nyboe Andersen A; ESHRE Reproduction and Society Task Force. Demographic and medical consequences of the postponement of parenthood［J］. Hum Reprod Update, 2012,18(1):29-43.
［6］Crider KS, Olney RS, Cragan JD. Trisomies 13 and 18: population prevalences, characteristics, and prenatal diagnosis, metropolitan Atlanta, 1994-2003［J］. Am J Med Genet A, 2008,146(7):820-826.
［8］Yamanaka M, Setoyama T, Igarashi Y, Kurosawa K, Itani Y, Hashimoto S, et al. Pregnancy outcome of fetuses with trisomy 18 identified by prenatal sonography and chromosomal analysis in a perinatal center［J］. Am J Med Genet, 2006,140(11): 1177-1182.
［9］Vendola C, Canfield M, Daiger SP, Gambello M, Hashmi SS, King T, et al: Survival of Texas infants born with trisomies 21, 18, and 13［J］. Am J Med Genet, 2010, 152A(2): 360-366.
［10］Chen CP, Su YN, Hsu CY, Ling PY, Tsai FJ, Chern SR, et al. Second-trimester molecular prenatal diagnosis of sporadic apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18［J］. Taiwan J Obstet Gynecol, 2010, 49(1):129-132.
［11］Irving C, Richmond S, Wren C, Longster C, Embleton ND. Changes in fetal prevalence and outcome for trisomies 13 and 18: a population-based study over 23 years［J］. J Matern Fetal Neonatal Med, 2011,24(1):137-141.
［12］De Souza E, Halliday J, Chan A, Bower C, Morris JK. Recurrence risks for trisomies 13, 18, and 21［J］. Am J Med Genet, 2009,149A(12):2716-2722.
［13］Seller MJ, Fear C, Kumar A, Mohammed S. Trisomy 16 in a mid-trimester IVF foetus with multiple Abnormalities［J］. Clin Dysmorphol, 2004,13(3):187-189.
［14］Hiroyuki Tateno. Chromosome aberrations in mouse embryos and fetuses produced by assisted reproductive technology［J］. Mutat Res, 2008,657(1):26-31.
［15］Santiago Munné. Preimplantation genetic diagnosis for aneuploidy and translocations using array comparative genomic hybridization［J］. Curr Genom, 2012,13(6):463-470.
［16］Chiamchanya C, Visutakul P, Gumnarai N, Su-angkawatin W. Preimplantation genetic screening (PGS) in infertile female age≥35 years by fluorescence in situ hybridization of chromosome 13, 18, 21, X and Y［J］. J Med Assoc Thai, 2008, 91(11): 1644-1650.
［17］van Landingham S, Bienstock J, Denne EW, Hueppchen N. Beyond the first trimester screen: Can we predict who will choose invasive testing?［J］. Genet Med, 2011,13(6):539-544.
