Article info
Original article
Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis
- Correspondence to Brigitte H W Faas, Department of Human Genetics, Radboud University Nijmegen Medical Centre, PO Box 9101, 6500 HB Nijmegen, The Netherlands; b.faas{at}antrg.umcn.nl
Citation
Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis
Publication history
- Received December 8, 2009
- Revised January 27, 2010
- Accepted February 1, 2010
- First published June 24, 2010.
Online issue publication
April 27, 2016
Article Versions
- Previous version (27 April 2016).
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© 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.