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Comprehensive diagnosis of Rett’s syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients
  1. Correspondence to:
 E Gak
 Danek Gertner Institute of Human Genetics, Sheba Medical Center, Tel Hashomer 52621, Israel; Eva.Gak{at}sheba.health.gov.il
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Citation

Petel-Galil Y, Ben-Zeev B, Greenbaum I, et al
Comprehensive diagnosis of Rett’s syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients

Publication history

  • Received January 26, 2006
  • Accepted May 20, 2006
  • Revised May 17, 2006
  • First published December 1, 2006.
Online issue publication 
April 27, 2016

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