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High frequency of genomic deletions—and a duplication—in the LIS1 gene in lissencephaly: implications for molecular diagnosis
  1. Professor R Guerrini, Pediatric Neurology Unit and Laboratories, Children’s Hospital A. Meyer – University of Florence, Viale Pieraccini 24, 50139 Firenze, Italy; r.guerrini{at}meyer.it
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Mei D, Lewis R, Parrini E, et al
High frequency of genomic deletions—and a duplication—in the LIS1 gene in lissencephaly: implications for molecular diagnosis

Publication history

  • Received November 27, 2007
  • Revised January 22, 2008
  • Accepted January 25, 2008
  • First published February 19, 2008.
Online issue publication 
June 02, 2008

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