Article info
Original article
Mutation in IFT80 in a fetus with the phenotype of Verma-Naumoff provides molecular evidence for Jeune-Verma-Naumoff dysplasia spectrum
- 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
Citation
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
January 27, 2011
Article Versions
- Previous version (30 July 2009).
- Previous version (11 August 2009).
- Previous version (7 January 2011).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
© 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.