Women's uptake of non-invasive DNA testing following a high-risk screening test for trisomy 21 within a publicly funded healthcare system: findings from a retrospective review-Reference-Cited by-同舟云学术

Women's uptake of non-invasive DNA testing following a high-risk screening test for trisomy 21 within a publicly funded healthcare system: findings from a retrospective review

Published:2015-01-04 Issue:4 Volume:35 Page:342-347
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Chan Yiu Man¹,Leung Wing Cheong²,Chan Wan Pang³,Leung Tak Yeung¹,Cheng Yvonne Kwun Yue¹,Sahota Daljit Singh¹

Affiliation:

1. Department of Obstetrics and Gynaecology; The Chinese University of Hong Kong; Shatin Hong Kong SAR China

2. Department of Obstetrics and Gynaecology; Kwong Wah Hospital; Kowloon Hong Kong SAR China

3. Department of Obstetrics and Gynaecology; Princess Margaret Hospital; Kowloon Hong Kong SAR China

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference22 articles.

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2. Risk factors for procedure-related fetal losses after mid-trimester genetic amniocentesis;Kong;Prenat Diagn,2006

3. Outcome of 1,355 consecutive transabdominal chorionic villus samplings in 1,351 patients;Lau;Chin Med J (Engl),2005

4. Chorion villus sampling versus amniocentesis for prenatal diagnosis;Alfirevic;Cochrane Database Syst Rev,2000

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