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Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function
- Maximilian Muenke, MD, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, 35 Convent Drive, MSC 3717, Building 35, Room 1B-203, Bethesda, MD 20892-3717; mamuenke{at}mail.nih.gov
Citation
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function
Publication history
- Received October 31, 2008
- Revised December 23, 2008
- Accepted January 21, 2009
- First published April 2, 2009.
Online issue publication
April 27, 2016
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- Previous version (27 April 2016).
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Web only appendices 46;6:389-398
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2009 BMJ Publishing Group Ltd