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Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals

Authors

  1. Correspondence to Maximilian Muenke, National Institutes of Health, Building 35, Room 1B-203, Bethesda, MD 20892, USA; mamuenke{at}mail.nih.gov
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Citation

Solomon BD, Lacbawan F, Mercier S, et al
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 
December 29, 2016

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