Implementing non-invasive prenatal testing into publicly funded antenatal screening services for Down syndrome and other conditions in Aotearoa New Zealand
Author:
Funder
Lotteries Health Research Grant
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynaecology
Link
http://link.springer.com/content/pdf/10.1186/s12884-017-1535-x.pdf
Reference33 articles.
1. Dondorp WJ, Page-Christiaens G, de Wert GM. Genomic futures of prenatal screening: ethical reflection. Clin Genet. 2016;89(5):531–8.
2. Thung DT, Beulen L, Hehir-Kwa J, Faas BH. Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories. Expert Rev Mol Diagn. 2015;15(1):111–24.
3. Wong AI, Lo YM. Noninvasive fetal genomic, methylomic, and transcriptomic analyses using maternal plasma and clinical implications. Trends Mol Med. 2015;21(2):98–108.
4. Wong FC, Lo YM. Prenatal Diagnosis Innovation: Genome Sequencing of Maternal Plasma. Annu Rev Med. 2016;67:419–32.
5. National Screening Unit. Antenatal Screening for Down Syndrome and Other Conditions: Guidelines for health practitioners. Wellington: Ministry of Health; 2012.
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