Syndromic Craniofacial Disorders
Author:
Publisher
Elsevier BV
Subject
Surgery
Reference56 articles.
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4. Craniosynostosis: Genes and mechanisms;Wilkie;Hum Mol Genet,1997
5. Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome;Lajeunie;Eur J Hum Genet,2006
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