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High frequency of genomic deletions—and a duplication—in the LIS1 gene in lissencephaly: implications for molecular diagnosis
- 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
Citation
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
April 27, 2016
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2008 BMJ Publishing Group Ltd