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Original article
Genotype–phenotype correlation in CC2D2A-related Joubert syndrome reveals an association with ventriculomegaly and seizures
  1. Correspondence to Dr Dan Doherty, Associate Professor, Divisions of Genetic Medicine and Developmental Medicine, University of Washington, Box 356320, RR-249, 1959 NE Pacific Street, Seattle, WA 98195-6320, USA; ddoher{at}uw.edu
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Citation

Bachmann-Gagescu R, Ishak GE, Dempsey JC, et al
Genotype–phenotype correlation in CC2D2A-related Joubert syndrome reveals an association with ventriculomegaly and seizures

Publication history

  • Received October 5, 2011
  • Revised December 7, 2011
  • Accepted December 8, 2011
  • First published January 12, 2012.
Online issue publication 
January 12, 2012

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