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FGFR2 mutation in a Chinese family with unusual Crouzon syndrome.
Li ZL, Chen X, Zhuang WJ, Zhao W, Liu YN, Zhang FX, Ha RS, Wu JH, Zhao C, Sheng XL. Li ZL, et al. Int J Ophthalmol. 2016 Oct 18;9(10):1403-1408. doi: 10.18240/ijo.2016.10.06. eCollection 2016. Int J Ophthalmol. 2016. PMID: 27803855 Free PMC article.
Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2.
Rong W, Chen X, Zhao K, Liu Y, Liu X, Ha S, Liu W, Kang X, Sheng X, Zhao C. Rong W, et al. Among authors: liu y, liu x, liu w. PLoS One. 2014 May 15;9(5):e97808. doi: 10.1371/journal.pone.0097808. eCollection 2014. PLoS One. 2014. PMID: 24831256 Free PMC article.
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