Syndromic craniosynostosis, fibroblast growth factor receptor 2 (FGFR2) mutations, and sacrococcygeal eversion presenting as human tails
Document Type
Journal Article
Publication Date
8-2012
Journal
Child's Nervous System
Volume
Volume 28, Issue 8
Inclusive Pages
1221-1226
Keywords
Abnormalities; Multiple--genetics; Acrocephalosyndactylia--genetics; Craniosynostoses--genetics; Receptor; Fibroblast Growth Factor; Type 2--genetics; Sacrococcygeal Region--abnormalities
APA Citation
Wilkinson, C.C., Manchester, D.K., Keating, R.F., Ketch, L.L., Winston, K.R. (2012). Syndromic craniosynostosis, fibroblast growth factor receptor 2 (FGFR2) mutations, and sacrococcygeal eversion presenting as human tails. Child's Nervous System, 28(8), 1221-1226.
Peer Reviewed
1
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