参考文献
1.Biesecker LG,Green RC.Diagnostic clinical genome and exome sequencing.N Engl J Med,2014,370(25):2418-2425.
2.Bodurtha J,Strauss JF 3rd.Genomics and perinatal care.N Engl JMed,2012,366(1):64-73.
3.Brambati B,Tului L.Chorionic villus sampling and amniocentesis.Curr Opin Obstet Gynecol,2005,17(2):197-201.
4.Collins FS,Varmus H.A new initiative on precision medicine.N Engl JMed,2015,372(9):793-795.
5.Dondorp W,deWert G,Bombard Y,et al.Non-invasive prenatal testing for aneuploidy and beyond:challengesof responsible innovation in prenatal screening.Eur JHum Genet,2015,23(11):1438-1450.
6.Ginsburg D.Genetics and genomics to the clinic:a long road ahead.Cell,2011,147(1):17-19.
7.Kuliev A,Verlinsky Y.Preimp lantation diagnosis:a realistic option for assisted reproduction and genetic practice.Curr Opin Obstet Gynecol,2005,17(2):179-183.
8.Lo YM,Chan KC,Sun H,et al.Maternal plasma DNA sequencing reveals the genome-wide genetic andmutation- al profile of the fetus.Sci Transl Med,2010,2(61):61ra91.
9.Lu JT,Campeau PM,Lee BH.Genotype-phenotype correlation—promiscuity in the era of next-generation sequencing.N Engl JMed,2014,371(7):593-596.
10.Tucker T,Marra M,Friedman JM.Massively parallel sequencing:the next big thing in genetic medicine.Am J Hum Genet,2009,85(2):142-154.
11.www.genetests.org.