Further evidence that fibroblast growth factor receptor 2 mutations cause Antley-Bixler syndrome
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2001.tb00811.x/fullpdf
Reference8 articles.
1. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome;Wilkie;Nature Genet,1995
2. Mutations in the fibroblast growth factor receptors: phenotypic consequences during eukaryotic development;Park;Am J Hum Genet,1995
3. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome;Reardon;Nature Genet,1994
4. FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome;Chun;Am J Med Genet,1998
5. Patient described by Chun et al. may not present Antley-Bixler syndrome;Gorlin;Am J Med Genet,1999
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