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本文引用的文献

1
Wrongful birth: clinical settings and legal implications.错误出生：临床情况与法律影响。
Semin Fetal Neonatal Med. 2014 Oct;19(5):312-6. doi: 10.1016/j.siny.2014.08.006. Epub 2014 Sep 1.
2
Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort.基于单核苷酸多态性的高危和低危队列的无创产前筛查。
Obstet Gynecol. 2014 Aug;124(2 Pt 1):210-218. doi: 10.1097/AOG.0000000000000363.
3
Noninvasive prenatal testing for microdeletion syndromes and expanded trisomies: proceed with caution.微缺失综合征和扩展三体的无创产前检测：谨慎行事。
Obstet Gynecol. 2014 May;123(5):1097-1099. doi: 10.1097/AOG.0000000000000237.
4
Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA.利用DNA大规模平行基因组测序技术对孕妇血液进行无创产前筛查，以检测胎儿21三体、18三体、13三体及常见性染色体非整倍体。
Am J Obstet Gynecol. 2014 Oct;211(4):365.e1-12. doi: 10.1016/j.ajog.2014.03.042. Epub 2014 Mar 19.
5
DNA sequencing versus standard prenatal aneuploidy screening.DNA 测序与标准产前非整倍体筛查。
N Engl J Med. 2014 Feb 27;370(9):799-808. doi: 10.1056/NEJMoa1311037.
6
Attitudes of mothers of children with down syndrome towards noninvasive prenatal testing.唐氏综合征患儿母亲对无创产前检测的态度
J Genet Couns. 2014 Oct;23(5):805-13. doi: 10.1007/s10897-014-9694-7. Epub 2014 Feb 1.
7
Next Generation sequencing is the impetus for the next generation of laboratory-based genetic counselors.新一代测序技术是新一代基于实验室的遗传咨询师的推动力。
J Genet Couns. 2014 Aug;23(4):647-54. doi: 10.1007/s10897-013-9684-1. Epub 2014 Jan 17.
8
Ethical and legal aspects of noninvasive prenatal genetic diagnosis.非侵入性产前基因诊断的伦理和法律问题。
Int J Gynaecol Obstet. 2014 Feb;124(2):181-4. doi: 10.1016/j.ijgo.2013.11.001. Epub 2013 Nov 14.
9
Obstetricians and gynecologists' practice and opinions of expanded carrier testing and noninvasive prenatal testing.妇产科医生对扩大携带者检测和无创产前检测的实践与看法。
Prenat Diagn. 2014 Feb;34(2):145-52. doi: 10.1002/pd.4272. Epub 2013 Dec 16.
10
Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.母体镶嵌是导致与无创性产前检测相关的性染色体非整倍体不一致的重要因素。
Clin Chem. 2014 Jan;60(1):251-9. doi: 10.1373/clinchem.2013.215145. Epub 2013 Nov 5.

Too much, too soon?: Commercial provision of noninvasive prenatal screening for subchromosomal abnormalities and beyond.

作者信息

Allyse Megan, Chandrasekharan Subhashini

机构信息

Biomedical Ethics Program, Mayo Clinic, Rochester, Minnesota, USA.

Duke Global Health Institute, Duke University, Durham, North Carolina, USA.

出版信息

Genet Med. 2015 Dec;17(12):958-61. doi: 10.1038/gim.2015.23. Epub 2015 Mar 19.

DOI:10.1038/gim.2015.23
PMID:25790161
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4993715/
Abstract
摘要