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Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss.
Wang H, Zhao Y, Yi Y, Gao Y, Liu Q, Wang D, Li Q, Lan L, Li N, Guan J, Yin Z, Han B, Zhao F, Zong L, Xiong W, Yu L, Song L, Yi X, Yang L, Petit C, Wang Q. Wang H, et al. Among authors: lan l. PLoS One. 2014 Aug 12;9(8):e103133. doi: 10.1371/journal.pone.0103133. eCollection 2014. PLoS One. 2014. PMID: 25116015 Free PMC article.
[Studies of the strategy for newborn gene screening].
Wang QJ, Zhao YL, Lan L, Zhao C, Han MK, Han DY. Wang QJ, et al. Among authors: lan l. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Nov;42(11):809-13. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18300440 Chinese.
[Audiological and genetic studies on 130 infants with hearing loss].
Wang DY, Wang QJ, Lan L, Shi W, Zhao C, Hui PL, Rao SQ, Han DY. Wang DY, et al. Among authors: lan l. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009 Mar;44(3):177-81. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009. PMID: 19558853 Chinese.
2,028 results