Holoprosencephaly and craniosynostosis: A report of two siblings and review of the literature
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference29 articles.
1. A hypomorphic allele in the FGF8 gene contributes to holoprosencephaly and is allelic to gonadotropin-releasing hormone deficiency in humans;Arauz;Molec Syndrom,2010
2. Primary craniosynostosis: Imaging features;Benson;Am J Roentgenol,1996
3. Holoprosencephaly and primary craniosynostosis: The Genoa syndrome;Camera;Am J Med Genet,1993
4. Sutural biology and the correlates of craniosynostosis;Cohen;Am J Med Genet,1993
5. Editorial: Perspectives on craniosynostosis;Cohen;Am J Med Genet Part A,2005
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