Author:
Hines Elizabeth A.,Jones Mary-Kayt N.,Harvey Julie F.,Perlyn Chad,Ornitz David M.,Sun Xin,Verheyden Jamie M.
Publisher
Springer Science and Business Media LLC
Subject
General Agricultural and Biological Sciences,General Environmental Science,General Biochemistry, Genetics and Molecular Biology
Reference20 articles.
1. Abler, L.L., Mehta, V., Keil, K.P., Joshi, P.S., Flucus, C.L., Hardin, H.A., Schmitz, C.T., and Vezina, C.M. (2011.) A high throughput in situ hybridization method to characterize mRNA expression patterns in the fetal mouse lower urogenital tract. J Vis Exp, doi: 10.3791/2912.
2. Apra, C., Collet, C., Arnaud, E., and Di Rocco, F. (2016). FGFR2 splice site mutations in Crouzon and Pfeiffer syndromes: two novel variants. Clin Genet 89, 746–748.
3. Cohen, M.M., and Kreiborg S. (1992). Birth prevalence studies of the Crouzon syndrome: comparison of direct and indirect methods. Clin Genet 41, 12–15.
4. Collet, C., Alessandri, J.L., Arnaud, E., Balu, M., Daire, V.C., and Di Rocco, F. (2014). Crouzon syndrome and Bent bone dysplasia associated with mutations at the same Tyr-381 residue in FGFR2 gene. Clin Genet 85, 598–599.
5. Eswarakumar, V.P., Horowitz, M.C., Locklin, R., Morriss-Kay, G.M., and Lonai, P. (2004). A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis. Proc Natl Acad Sci USA 101, 12555–12560.
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