Second-trimester prenatal screening for trisomy 21 using biochemical markers: a 7-year experience in one cytogenetic laboratory-Reference-Cited by-同舟云学术

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Second-trimester prenatal screening for trisomy 21 using biochemical markers: a 7-year experience in one cytogenetic laboratory

Published:2006 Issue:4 Volume:26 Page:308-312
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Marical Hélène,Douet-Guilbert Nathalie,Bages Karine,Collet Michel,Le Bris Marie-Josée,Morel Frédéric,De Braekeleer Marc

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference27 articles.

1. Dépistage de la trisomie 21 : clarté nucale et/ou marqueurs sériques ?

2. Prenatal diagnosis of diverse chromosome abnormalities in a population of patients identified by triple-marker testing as screen positive for Down syndrome

3. One-stop clinic for assessment of risk for trisomy 21 at 11-14 weeks: a prospective study of 15 030 pregnancies

4. A prospective trial of prenatal screening for Down syndrome by means of maternal serum α-fetoprotein, human chorionic gonadotropin, and unconjugated estriol

5. Frequencies of chromosomal abnormalities at amniocentesis: Over 20 years of cytogenetic analyses in one laboratory

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Maternal Serum Screening for Chromosomal Abnormalities and Neural Tube Defects;Genetic Disorders and the Fetus;2021-04-20

2. Maternal Serum Screening for Chromosomal Abnormalities and Neural Tube Defects;Genetic Disorders and the Fetus;2015-11-23

3. Screening for Down syndrome - incidental diagnosis of other aneuploidies;Prenatal Diagnosis;2014-06-11

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