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Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1
  1. Correspondence to:
 A Slavotinek
 Department of Pediatrics, University of California, San Francisco, 533 Parnassus St, Room U585P, San Francisco, CA 94143-0748, USA; slavotiapeds.ucsf.edu
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Citation

Slavotinek A, Lee SS, Davis R, et al
Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1

Publication history

  • Accepted January 20, 2005
  • Revised December 3, 2004
  • First published September 1, 2005.
Online issue publication 
April 27, 2016

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