References
- Ferencz C, Rubin JD, McCarter RJ, et al. Congenital heart disease: prevalence at livebirth. The Baltimore-Washington Infant Study. Am J Epidemiol. 1985;121(1):31–36.
- Hoffman JI. Incidence of congenital heart disease: I. Postnatal incidence. Pediatr Cardiol. 1995;16(3):103–113.
- Zhao QM, Ma XJ, Jia B, et al. Prevalence of congenital heart disease at live birth: an accurate assessment by echocardiographic screening. Acta Paediatr. 2013;102(4):397–402.
- Hoffman JI. Incidence of congenital heart disease: II. Prenatal incidence. Pediatr Cardiol. 1995;16(4):155–165.
- Paladini D. VP congenital fetal anomalies. Informa Healthcare; 2007.
- Harper PS Practical genetic counselling. 7th ed. Springer; 2010.
- Galindo A, Herraiz I, Escribano D, et al. Prenatal detection of congenital heart defects: a survey on clinical practice in Spain. Fetal Diagn Ther. 2011;29(4):287–295.
- Wapner RJ, Martin CL, Levy B, et al. Chromosomal microarray versus karyotyping for prenatal diagnosis. N Engl J Med. 2012;367(23):2175–2184.
- Donnelly JC, Platt LD, Rebarber A, et al. Association of copy number variants with specific ultrasonographically detected fetal anomalies. Obstet Gynecol. 2014;124(1):83–90.
- Shaffer LG, Rosenfeld JA, Dabell MP, et al. Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound. Prenat Diagn. 2012;32(10):986–995.
- Svirsky R, Reches A, Brabbing-Goldstein D, et al. Association of aberrant right subclavian artery with abnormal karyotype and microarray results. Prenat Diagn. 2017;37(8):808–811.
- Kearney HM, Thorland EC, Brown KK, et al. American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants. Genet Med. 2011;13(7):680–685.
- Bayes T. An essay towards solving a problem in the doctrine of chances. 1763. M D Comput. 1991;8(3):157–171.
- Kirk JS, Comstock CH, Lee W, et al. Sonographic screening to detect fetal cardiac anomalies: a 5-year experience with 111 abnormal cases. Obstet Gynecol. 1997;89(2):227–232.
- Mirza FG, Bauer ST, Williams IA, et al. Early fetal echocardiography: ready for prime time? Am J Perinatol. 2012;29(4):313–318.
- Garne E. Atrial and ventricular septal defects – epidemiology and spontaneous closure. J Matern Fetal Neonatal Med. 2006;19(5):271–276.
- Gómez O, Martínez JM, Olivella A, et al. Isolated ventricular septal defects in the era of advanced fetal echocardiography: risk of chromosomal anomalies and spontaneous closure rate from diagnosis to age of 1 year. Ultrasound Obstet Gynecol. 2014;43(1):65–71.
- Yan Y, Wu Q, Zhang L, et al. Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease. Ultrasound Obstet Gynecol. 2014;43(4):404–412.
- Mademont-Soler I, Morales C, Soler A, et al. Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis. Ultrasound Obstet Gynecol. 2013;41(4):375–382.
- Costain G, Silversides CK, Bassett AS. The importance of copy number variation in congenital heart disease. Npj Genom Med. 2016;1:16031.
- Du L, Xie HN, Huang LH, et al. Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with ventricular septal defects by chromosomal microarray-based analysis. Prenat Diagn. 2016;36(13):1178–1184.
- Takeichi T, Akiyama M. Inherited ichthyosis: non-syndromic forms. J Dermatol. 2016;43(3):242–251.
- Li X, Song GX, Wu LJ, et al. Prediction of spontaneous closure of isolated ventricular septal defects in utero and postnatal life. BMC Pediatr. 2016;16(1):207.