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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
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Copyright 2005 Journal of Medical Genetics