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Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis
  1. 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
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Faas BHW, van der Burgt I, Kooper AJA, et al
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

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