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Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals
- Correspondence to Maximilian Muenke, National Institutes of Health, Building 35, Room 1B-203, Bethesda, MD 20892, USA; mamuenke{at}mail.nih.gov
Citation
Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals
Publication history
- Received September 7, 2009
- Revised November 22, 2009
- Accepted November 24, 2009
- First published December 2, 2009.
Online issue publication
July 23, 2010
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© 2010, 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.