孕早期联合生化和超声筛查检测涉及常染色体和性染色体的双非整倍体。 - Suppr | 超能文献

First trimester detection of double aneuploidy involving autosomes and sex chromosomes using combined biochemical and ultrasound screening.

作者信息

Spencer Kevin

机构信息

Department of Clinical Biochemistry, King George Hospital, Goodmayes, UK.

出版信息

Prenat Diagn. 2013 Nov;33(11):1105-6. doi: 10.1002/pd.4192. Epub 2013 Jul 26.

DOI:10.1002/pd.4192

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

First trimester detection of double aneuploidy involving autosomes and sex chromosomes using combined biochemical and ultrasound screening.孕早期联合生化和超声筛查检测涉及常染色体和性染色体的双非整倍体。

Prenat Diagn. 2013 Nov;33(11):1105-6. doi: 10.1002/pd.4192. Epub 2013 Jul 26.

2

Current methods of prenatal screening for Down syndrome and other fetal abnormalities.目前唐氏综合征和其他胎儿异常的产前筛查方法。

Clin Obstet Gynecol. 2008 Mar;51(1):24-36. doi: 10.1097/GRF.0b013e318160f274.

3

The use of prenatal ultrasound for the detection of fetal aneuploidy.产前超声用于检测胎儿非整倍体。

Clin Obstet Gynecol. 2008 Mar;51(1):48-61. doi: 10.1097/GRF.0b013e31816163e3.

4

Early vaginal bleeding has no impact on markers used in first trimester aneuploidy screening.早期阴道出血对早孕期非整倍体筛查标志物无影响。

Prenat Diagn. 2010 Jun;30(6):547-50. doi: 10.1002/pd.2519.

5

New trends in prenatal screening for chromosomal abnormalities.染色体异常产前筛查的新趋势。

Saudi Med J. 2000 May;21(5):429-32.

6

Non-invasive chromosome test raises new questions in prenatal diagnosis about the significance of ultrasound and questions about new screening strategies.无创染色体检测在产前诊断中引发了关于超声意义的新问题以及新筛查策略的问题。

Ultraschall Med. 2013 Oct;34(5):417-20. doi: 10.1055/s-0033-1350597. Epub 2013 Oct 14.

7

[Fetal diagnosis from the mother's blood--noninvasive screening of chromosomal aberrations].[从母亲血液中进行胎儿诊断——染色体畸变的无创筛查]

Duodecim. 2015;131(22):2083-8.

8

[Clinical application of noninvasive prenatal diagnosis using cell free fetal DNA in maternal plasma].游离胎儿DNA在母体血浆中用于无创产前诊断的临床应用

Zhonghua Fu Chan Ke Za Zhi. 2012 Nov;47(11):813-7.

9

Does timing of biochemistry in first-trimester aneuploidy risk assessment affect the gestational age at prenatal diagnosis and pregnancy termination?早孕期三体风险评估时生物化学标志物检测时间是否会影响产前诊断和终止妊娠的孕周？

Prenat Diagn. 2010 Dec;30(12-13):1151-4. doi: 10.1002/pd.2630.

10

Contribution of "modified genetic sonography" to the combined test as a screening method for chromosomal abnormalities.

J Matern Fetal Neonatal Med. 2012 Aug;25(8):1399-405. doi: 10.3109/14767058.2011.636100. Epub 2011 Nov 30.

引用本文的文献

1

Placental Histomorphology in a Case of Double Trisomy 48,XXX,+18.一例48,XXX,+18双三体病例的胎盘组织形态学

Case Rep Pathol. 2018 Mar 8;2018:2839765. doi: 10.1155/2018/2839765. eCollection 2018.

2

Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnoses.全染色体非整倍体且伴有疑似或确诊的第二种诊断的患者的表型改变。

Am J Med Genet A. 2015 Sep;167A(9):2168-75. doi: 10.1002/ajmg.a.37126. Epub 2015 Apr 25.