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Nonsyndromic craniosynostosis: novel coding variants.
Sewda A, White SR, Erazo M, Hao K, García-Fructuoso G, Fernández-Rodriguez I, Heuzé Y, Richtsmeier JT, Romitti PA, Reva B, Jabs EW, Peter I. Sewda A, et al. Among authors: jabs ew. Pediatr Res. 2019 Mar;85(4):463-468. doi: 10.1038/s41390-019-0274-2. Epub 2019 Jan 14. Pediatr Res. 2019. PMID: 30651579 Free PMC article.
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. Among authors: jabs ew. Dev Dyn. 2010 Mar;239(3):987-97. doi: 10.1002/dvdy.22218. Dev Dyn. 2010. PMID: 20077479 Free PMC article.
Associations between periconceptional alcohol consumption and craniosynostosis, omphalocele, and gastroschisis.
Richardson S, Browne ML, Rasmussen SA, Druschel CM, Sun L, Jabs EW, Romitti PA; National Birth Defects Prevention Study. Richardson S, et al. Among authors: jabs ew. Birth Defects Res A Clin Mol Teratol. 2011 Jul;91(7):623-30. doi: 10.1002/bdra.20823. Epub 2011 May 31. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21630421 Free PMC article.
p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice.
Wang Y, Zhou X, Oberoi K, Phelps R, Couwenhoven R, Sun M, Rezza A, Holmes G, Percival CJ, Friedenthal J, Krejci P, Richtsmeier JT, Huso DL, Rendl M, Jabs EW. Wang Y, et al. Among authors: jabs ew. J Clin Invest. 2012 Jun;122(6):2153-64. doi: 10.1172/JCI62644. Epub 2012 May 15. J Clin Invest. 2012. PMID: 22585574 Free PMC article.
HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice.
Webb BD, Shaaban S, Gaspar H, Cunha LF, Schubert CR, Hao K, Robson CD, Chan WM, Andrews C, MacKinnon S, Oystreck DT, Hunter DG, Iacovelli AJ, Ye X, Camminady A, Engle EC, Jabs EW. Webb BD, et al. Among authors: jabs ew. Am J Hum Genet. 2012 Jul 13;91(1):171-9. doi: 10.1016/j.ajhg.2012.05.018. Epub 2012 Jul 5. Am J Hum Genet. 2012. PMID: 22770981 Free PMC article.
256 results