Chen H - Search Results

1

[An investigation of SLC26A4 gene mutation in nonsydromic hearing impairment in Hunan province of China].

Jiang L, Feng Y, Chen H, He C, Mei L. Jiang L, et al. Among authors: chen h. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010 Jul;24(13):587-91. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010. PMID: 20842945 Chinese.

2

Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome.

Chen H, Jiang L, Xie Z, Mei L, He C, Hu Z, Xia K, Feng Y. Chen H, et al. Biochem Biophys Res Commun. 2010 Jun 18;397(1):70-4. doi: 10.1016/j.bbrc.2010.05.066. Epub 2010 May 15. Biochem Biophys Res Commun. 2010. PMID: 20478267

3

Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndrome.

Jiang L, Chen H, Jiang W, Hu Z, Mei L, Xue J, He C, Liu Y, Xia K, Feng Y. Jiang L, et al. Among authors: chen h. Biochem Biophys Res Commun. 2011 May 20;408(4):620-4. doi: 10.1016/j.bbrc.2011.04.072. Epub 2011 Apr 21. Biochem Biophys Res Commun. 2011. PMID: 21531202

4

Gene localization in a Chinese family with autosomal dominant non-syndromic deafness.

Jiang L, Liu Y, Feng Y, Hu Z, Mei L, Long L, Chen H, Xue J, Xia K, He C. Jiang L, et al. Among authors: chen h. Acta Otolaryngol. 2011 Oct;131(10):1061-8. doi: 10.3109/00016489.2011.591822. Epub 2011 Jun 8. Acta Otolaryngol. 2011. PMID: 21651318

5

Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II.

Zhang H, Chen H, Luo H, An J, Sun L, Mei L, He C, Jiang L, Jiang W, Xia K, Li JD, Feng Y. Zhang H, et al. Among authors: chen h. Hum Genet. 2012 Mar;131(3):491-503. doi: 10.1007/s00439-011-1098-2. Epub 2011 Oct 1. Hum Genet. 2012. PMID: 21965087

6

Functional analysis of MITF gene mutations associated with Waardenburg syndrome type 2.

Zhang H, Luo H, Chen H, Mei L, He C, Jiang L, Li JD, Feng Y. Zhang H, et al. Among authors: chen h. FEBS Lett. 2012 Nov 30;586(23):4126-31. doi: 10.1016/j.febslet.2012.10.006. Epub 2012 Oct 23. FEBS Lett. 2012. PMID: 23098757 Free article.

7

Identification and functional analysis of a novel mutation in the SOX10 gene associated with Waardenburg syndrome type IV.

Wang HH, Chen HS, Li HB, Zhang H, Mei LY, He CF, Wang XW, Men MC, Jiang L, Liao XB, Wu H, Feng Y. Wang HH, et al. Among authors: chen hs. Gene. 2014 Mar 15;538(1):36-41. doi: 10.1016/j.gene.2014.01.026. Epub 2014 Jan 16. Gene. 2014. PMID: 24440785

8

Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.

Wang H, Wang X, He C, Li H, Qing J, Grati M, Hu Z, Li J, Hu Y, Xia K, Mei L, Wang X, Yu J, Chen H, Jiang L, Liu Y, Men M, Zhang H, Guan L, Xiao J, Zhang J, Liu X, Feng Y. Wang H, et al. Among authors: chen h. J Hum Genet. 2015 Mar;60(3):119-126. doi: 10.1038/jhg.2014.114. Epub 2015 Jan 15. J Hum Genet. 2015. PMID: 25589040 Free PMC article.

9

[Construction and analysis of recombinant eukaryotic expression plasmids for SOX10, the causative gene of Warrdenburg syndrome].

Zhang H, Feng J, Chen H, Li J, Luo H, Feng Y. Zhang H, et al. Among authors: chen h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):49-55. doi: 10.3760/cma.j.issn.1003-9406.2015.01.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25636099 Chinese.

10

[The analysis of nystagmus in patients with posterior canal benign paroxysmal positional vertigoin positioning test].

Cui X, Feng Y, Mei L, He C, Lu X, Zhang H, Chen H. Cui X, et al. Among authors: chen h. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2015 Jan;29(1):27-30. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2015. PMID: 25966550 Chinese.

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