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  • Epigenetic mutations of the imprinted IGF2-H19 domain in Silver–Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes

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Epigenetic mutations of the imprinted IGF2-H19 domain in Silver–Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes

Authors

  1. Dr D Bartholdi, Institute of Medical Genetics, University of Zürich, Schorenstrasse 16, 8603 Schwerzenbach, Switzerland; debobarth{at}yahoo.com
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Citation

Bartholdi D, Krajewska-Walasek M, Õunap K, et al
Epigenetic mutations of the imprinted IGF2-H19 domain in Silver–Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes
Journal of Medical Genetics 2009;46:192-197.

Publication history

  • Received August 3, 2008
  • Revised November 15, 2008
  • Accepted November 19, 2008
  • First published December 9, 2008.
Online issue publication 
April 27, 2016

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2009 BMJ Publishing Group Ltd