Syndromic craniosynostosis, fibroblast growth factor receptor 2 (FGFR2) mutations, and sacrococcygeal eversion presenting as human tails
Document Type
Journal Article
Publication Date
2012
Journal
Child's Nervous System
Inclusive Pages
1221-1226
APA Citation
Wilkinson, C., Manchester, D., Keating, R., & Ketch, L. (2012). Syndromic craniosynostosis, fibroblast growth factor receptor 2 (FGFR2) mutations, and sacrococcygeal eversion presenting as human tails. Child's Nervous System, (). Retrieved from https://hsrc.himmelfarb.gwu.edu/smhs_neurosurg_facpubs/299
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