Advances in the prenatal diagnosis of monogenic disorders

Prenatal DiagnosisVolume 38, Issue 1 p. 3-5 Editorial Advances in the prenatal diagnosis of monogenic disorders Lyn S. Chitty, Corresponding Author Lyn S. Chitty l.chitty@ucl.ac.uk orcid.org/0000-0002-4857-7138 Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UKCorrespondence to: Lyn S. Chitty. E-mail: l.chitty@ucl.ac.ukSearch for more papers by this author Lyn S. Chitty, Corresponding Author Lyn S. Chitty l.chitty@ucl.ac.uk orcid.org/0000-0002-4857-7138 Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UKCorrespondence to: Lyn S. Chitty. E-mail: l.chitty@ucl.ac.ukSearch for more papers by this author First published: 21 February 2018 https://doi.org/10.1002/pd.5208Citations: 8Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume38, Issue1Special Issue: Special topic issue on advances in the diagnosis of single gene disordersJanuary 2018Pages 3-5 RelatedInformation