These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
8. Craniosynostosis-associated Fgfr2(C342Y) mutant bone marrow stromal cells exhibit cell autonomous abnormalities in osteoblast differentiation and bone formation. Liu J, Kwon TG, Nam HK, Hatch NE. Biomed Res Int; 2013 Apr; 2013():292506. PubMed ID: 23762837 [Abstract] [Full Text] [Related]
9. Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings. Agochukwu NB, Solomon BD, Muenke M. Int J Pediatr Otorhinolaryngol; 2014 Dec; 78(12):2037-47. PubMed ID: 25441602 [Abstract] [Full Text] [Related]
10. 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. J Clin Invest; 2012 Jun; 122(6):2153-64. PubMed ID: 22585574 [Abstract] [Full Text] [Related]
13. Dura in the pathogenesis of syndromic craniosynostosis: fibroblast growth factor receptor 2 mutations in dural cells promote osteogenic proliferation and differentiation of osteoblasts. Ang BU, Spivak RM, Nah HD, Kirschner RE. J Craniofac Surg; 2010 Mar; 21(2):462-7. PubMed ID: 20489451 [Abstract] [Full Text] [Related]
19. Mandibular dysmorphology due to abnormal embryonic osteogenesis in FGFR2-related craniosynostosis mice. Motch Perrine SM, Wu M, Stephens NB, Kriti D, van Bakel H, Jabs EW, Richtsmeier JT. Dis Model Mech; 2019 May 30; 12(5):. PubMed ID: 31064775 [Abstract] [Full Text] [Related]
20. A Case of Beare-Stevenson Syndrome with Unusual Manifestations. Ron N, Leung S, Carney E, Gerber A, David KL. Am J Case Rep; 2016 Apr 15; 17():254-8. PubMed ID: 27079505 [Abstract] [Full Text] [Related] Page: [Next] [New Search]