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Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function
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Authors

  1. 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
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Citation

Lacbawan F, Solomon BD, Roessler E, et al
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 
June 01, 2009

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