Mutation detection in FGFR2 craniosynostosis syndromes

• 27 January 1997
• journal article
• case report
• Published by Springer Nature in Human Genetics
• Vol. 99  (2) , 251-255
• https://doi.org/10.1007/s004390050348

Abstract

Keywords

• MUTATIONS
• FGFR2
• EXONS
• CROUZON SYNDROME
• PFEIFFER
• IIIC
• CRANIOSYNOSTOSIS SYNDROMES