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Brain phenotypes in two FGFR2 mouse models for Apert syndrome.
Aldridge K, Hill CA, Austin JR, Percival C, Martinez-Abadias N, Neuberger T, Wang Y, Jabs EW, Richtsmeier JT. Aldridge K, et al. Dev Dyn. 2010 Mar;239(3):987-97. doi: 10.1002/dvdy.22218. Dev Dyn. 2010. PMID: 20077479 Free PMC article.
Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes.
Heuzé Y, Martínez-Abadías N, Stella JM, Arnaud E, Collet C, García Fructuoso G, Alamar M, Lo LJ, Boyadjiev SA, Di Rocco F, Richtsmeier JT. Heuzé Y, et al. Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):250-9. doi: 10.1002/bdra.23228. Epub 2014 Feb 27. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 24578066 Free PMC article. Clinical Trial.
43 results