Mild isolated craniosynostosis due to a novel FGFR3 mutation, p.Ala334Thr

Author:

Barroso Eva,Pérez-Carrizosa Virginia,García-Recuero Ignacio,Glucksman Marc J.,Wilkie Andrew O.,García-Minaur Sixto,Heath Karen E.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference16 articles.

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3. Fibroblast growth factor 1 induced during myogenesis by a transcription-translation coupling mechanism;Conte;Nucleic Acids Res,2009

4. Craniosynostosis;Johnson;Eur J Hum Genet,2011

5. A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome;Muenke;Am J Hum Genet,1997

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