Article info
Original article
Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development
- Correspondence to: T Attié-Bitach Département de Génétique et Unité INSERM U-393, Hôpital Necker-Enfants Malades, 149, rue de Sèvres, 75743 Paris Cedex 15, France; tania.attie{at}necker.fr
Citation
Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development
Publication history
- Accepted August 18, 2005
- Revised August 11, 2005
- First published September 16, 2005.
Online issue publication
March 08, 2006
Article Versions
- Previous version (16 September 2005).
- Previous version (23 September 2005).
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Copyright information
Copyright 2006 Journal of Medical Genetics