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Mutation in IFT80 in a fetus with the phenotype of Verma-Naumoff provides molecular evidence for Jeune-Verma-Naumoff dysplasia spectrum
  1. Correspondence to Prof Denise P Cavalcanti, Programa de Genética Perinatal, Depto. de Genética Médica, FCM, UNICAMP, CP 6111, 13081-970, Campinas, SP Brazil; denisepc{at}unicamp.br denisepcavalcanti{at}gmail.com
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Cavalcanti DP, Huber C, Le Quan Sang K, et al
Mutation in IFT80 in a fetus with the phenotype of Verma-Naumoff provides molecular evidence for Jeune-Verma-Naumoff dysplasia spectrum

Publication history

  • Received May 18, 2009
  • Revised July 1, 2009
  • Accepted July 2, 2009
  • First published July 30, 2009.
Online issue publication 
April 27, 2016

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