Article info
Online mutation report
First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutations
- Correspondence to: Dr S Odent Unité de Génétique Médicale, Hôpital SUD, 16 Bd de Bulgarie BP 90347, 35203 Rennes cedex 2, France; sylvie.odentchu-rennes.fr
Citation
First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutations
Publication history
- Received August 27, 2004
- Accepted September 1, 2004
- First published January 5, 2005.
Online issue publication
January 05, 2005
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
Copyright 2005 Journal of Medical Genetics