Opening Pandora's box?: ethical issues in prenatal whole genome and exome sequencing
Author:
Affiliation:
1. The Ethox Centre; University of Oxford; Oxford UK
Funder
Health Innovation Challenge Fund
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.5114/fullpdf
Reference60 articles.
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3. Deciphering developmental disorders study. Prevalence and architecture of de novo mutations in developmental disorders;Nature,2017
4. Promises, pitfalls and practicalities of prenatal whole exome sequencing;Best;Prenat Diagn,2017
5. Non-invasive whole genome sequencing of a human fetus;Kitzman;Sci Transl Med,2012
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