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Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome
  1. Correspondence to:
 Dr A Rauch, Institut für Humangenetik, Schwabachanlage 10, 91054 Erlangen, Germany; 
 arauch{at}humgenet.uni-erlangen.de
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Citation

Zweier C, Temple IK, Beemer F, et al
Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome

Publication history

  • First published August 14, 2003.
Online issue publication 
April 27, 2016

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