孕早期胎儿21三体综合征的诊断 - Suppr

Suppr

超能文献

Diagnosis of fetal trisomy 21 in first trimester.

作者信息

Brambati B, Simoni G

出版信息

Lancet. 1983 Mar 12;1(8324):586.

PMID:6131275

Abstract

摘要

相似文献

Diagnosis of fetal trisomy 21 in first trimester.

Lancet. 1983 Mar 12;1(8324):586.

First-trimester screening for trisomy 21 combining biochemistry and ultrasound at individually optimal gestational ages. An interventional study.

Prenat Diagn. 2004 Jul;24(7):541-5. doi: 10.1002/pd.949.

The significance of fetal maxillary length in the first trimester screening for trisomy 21.

Arch Gynecol Obstet. 2011 Jun;283(6):1199-205. doi: 10.1007/s00404-010-1527-9. Epub 2010 May 28.

[Value of detection of cell-free fetal DNA in maternal plasma in the prenatal diagnosis of chromosomal abnormalities].

Zhonghua Fu Chan Ke Za Zhi. 2012 Nov;47(11):808-12.

First-trimester screening for trisomy 21 in Denmark: implications for detection and birth rates of trisomy 18 and trisomy 13.

Ultrasound Obstet Gynecol. 2011 Aug;38(2):140-4. doi: 10.1002/uog.8929.

Performance of first-trimester serum screening for trisomy 21 before and from 11 + 0 weeks of gestational age in The Netherlands.

Prenat Diagn. 2010 Sep;30(9):906-8. doi: 10.1002/pd.2581.

Multicenter study of first-trimester screening for trisomy 21 in 75 821 pregnancies: results and estimation of the potential impact of individual risk-orientated two-stage first-trimester screening.

Ultrasound Obstet Gynecol. 2005 Mar;25(3):221-6. doi: 10.1002/uog.1860.

Fetal hydrops and hepatosplenomegaly in the second half of pregnancy: a sign of myeloproliferative disorder in fetuses with trisomy 21.

Ultrasound Obstet Gynecol. 2001 May;17(5):403-9. doi: 10.1046/j.1469-0705.2001.00384.x.

First-trimester tests for trisomies 21 and 18 as sensitive as triple screen.

J Fam Pract. 2004 Mar;53(3):184-6.

A screening program for trisomy 21 at 10-14 weeks using fetal nuchal translucency, maternal serum free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A.

Ultrasound Obstet Gynecol. 1999 Apr;13(4):231-7. doi: 10.1046/j.1469-0705.1999.13040231.x.

引用本文的文献

Prenatal Management of Spinal Muscular Atrophy in the Era of Genetic Screening and Emerging Opportunities in In Utero Therapy.

Biomedicines. 2025 Jul 22;13(8):1796. doi: 10.3390/biomedicines13081796.

Genetic variation in placental insufficiency: What have we learned over time?

Front Cell Dev Biol. 2022 Oct 14;10:1038358. doi: 10.3389/fcell.2022.1038358. eCollection 2022.

A 26-Year Experience in Chorionic Villus Sampling Prenatal Genetic Diagnosis.

J Clin Med. 2014 Jul 24;3(3):838-48. doi: 10.3390/jcm3030838.

Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis.

J Clin Med. 2014 Jul 24;3(3):809-37. doi: 10.3390/jcm3030809.

Human molecular cytogenetics: From cells to nucleotides.

Genet Mol Biol. 2014 Mar;37(1 Suppl):194-209. doi: 10.1590/s1415-47572014000200006.

First trimester fetal karyotyping in twin pregnancy.

J Med Genet. 1984 Feb;21(1):58-60. doi: 10.1136/jmg.21.1.58.

DNA analysis of first-trimester chorionic villous biopsies: test for maternal contamination.

Am J Hum Genet. 1984 Nov;36(6):1357-68.

First-trimester prenatal diagnosis of mucolipidosis II (I-cell disease) by chorionic biopsy.

Am J Hum Genet. 1984 Nov;36(6):1379-85.

Diagnostic application of first trimester trophoblast sampling in 100 pregnancies.

Hum Genet. 1984;66(2-3):252-9. doi: 10.1007/BF00286612.

Method of sampling chorionic villi in first trimester of pregnancy under guidance of real time ultrasound.

Br Med J (Clin Res Ed). 1983 May 14;286(6377):1542-4. doi: 10.1136/bmj.286.6377.1542.

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。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验