Literature DB >> 18049087

A mutation in FGFR2 in a child with Pfeiffer syndrome and a sacral appendage.

Angeline H M Lai1, Yuen-Ming Tan, Hai-Yang Law, Vincent K L Yeow.   

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Year:  2008        PMID： 18049087     DOI： 10.1097/MCD.0b013e3282efdaf1

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  1 in total

Review 1.  Syndromic craniosynostosis, fibroblast growth factor receptor 2 (FGFR2) mutations, and sacrococcygeal eversion presenting as human tails.

Authors:  C Corbett Wilkinson; David K Manchester; Robert F Keating; Lawrence L Ketch; Ken R Winston
Journal:  Childs Nerv Syst       Date:  2012-06-04       Impact factor: 1.475
  1 in total

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