First trimester screening for trisomy 18 by a combination of nuchal translucency thickness and epigenetic marker level-Reference-Cited by-同舟云学术

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First trimester screening for trisomy 18 by a combination of nuchal translucency thickness and epigenetic marker level

Published:2017-06-30 Issue:1 Volume:14 Page:1-7
ISSN:1226-1769
Container-title:Journal of Genetic Medicine
language:en
Short-container-title:J Genet Med

Author:

Lee Da Eun¹,Kim Shin Young¹,Kim Hyun Jin¹,Park So Yeon¹,Kim Min Hyoung²,Han You Jung²,Ryu Hyun Mee¹²

Affiliation:

1. Laboratory of Medical Genetics, Medical Research Institute, Cheil General Hospital and Women’s Healthcare Center, Seoul, Korea

2. Department of Obstetrics and Gynecology, Cheil General Hospital and Women’s Healthcare Center, Dankook University College of Medicine, Seoul, Korea

Funder

Ministry of Health and Welfare(Ministry of Health, Welfare and Family Affairs)

Publisher

Korean Society of Medical Genetics

Subject

General Medicine

Link

http://pdf.medrang.co.kr/JGM/2017/014/JGM014-01-01.pdf

Reference25 articles.

1. Fetal Mild Hydronephrosis and Chromosomal Defects: Relation to Maternal Age and Gestation

2. Detection of trisomy 18 and trisomy 13 using first and second trimester Down's syndrome screening markers

3. UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10–14 weeks of gestation

4. Screening performance of first-trimester nuchal translucency for major cardiac defects: a meta-analysis

5. Morphological classification of nuchal skin in human fetuses with trisomy 21, 18, and 13 at 12--18 weeks and in a trisomy 16 mouse

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