Article info

Download PDFPDF
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis

Authors

  1. Dr B B A de Vries, Department of Human Genetics 849, RUNMC, PO Box 9101 6500 HB Nijmegen, The Netherlands; b.devries{at}antrg.umcn.nl
View Full Text

Citation

van Bon BWM, Koolen DA, Borgatti R, et al
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis

Publication history

  • Received October 31, 2007
  • Revised December 11, 2007
  • Accepted December 12, 2007
  • First published January 4, 2008.
Online issue publication 
December 29, 2016

Article Versions

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.