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.
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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.