He CF - Search Results

1

Digenic mutations involving both the BSND and GJB2 genes detected in Bartter syndrome type IV.

Wang HH, Feng Y, Li HB, Wu H, Mei LY, Wang XW, Jiang L, He CF. Wang HH, et al. Among authors: he cf. Int J Pediatr Otorhinolaryngol. 2017 Jan;92:17-20. doi: 10.1016/j.ijporl.2016.10.028. Epub 2016 Oct 26. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28012523

2

[An analysis of a large hereditary postlingually deaf families and detecting mutation of the deafness genes].

Feng Y, He Cf, Xiao J, Fang J, Zhao S, Tian X, Mei L, Xia K, Tang X. Feng Y, et al. Among authors: he cf. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2002 Jul;16(7):323-5. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2002. PMID: 15510726 Chinese.

3

[Mutation analysis of gene CX31.1 in the hereditary hearing loss pedigrees].

Feng Y, He C, Xia K, Li Q, He D. Feng Y, et al. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2005 Feb;19(4):178-9. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2005. PMID: 15938215 Chinese.

4

[The prenatal diagnosis and early intervention of nonsyndromic hearing loss of connexin26 gene].

He C, Feng Y, Xia K, Mei L, He D. He C, et al. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006 Jul;20(13):579-81. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006. PMID: 16981465 Chinese.

5

[The application of 3D reconstruction of CT scans for the observation of the cochlear implanted electrode location].

Liu H, Feng Y, Chen D, CaI X, He C. Liu H, et al. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006 Jul;20(13):597-9. Lin Chuang Er Bi Yan Hou Ke Za Zhi. 2006. PMID: 16981471 Chinese.

6

[Surgical approaches and related microsurgical anatomy about suprameatal approach: new surgical approach for cochlear implantation].

Liu H, Feng Y, Chen D, Mei L, He C, Cai X. Liu H, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 May;21(10):447-9. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17650813 Chinese.

7

[Screening and identification interaction proteins of connexin 30].

He DH, Feng Y, Mei LY, He CF. He DH, et al. Among authors: he cf. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009 Sep;44(9):758-61. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009. PMID: 20079101 Chinese.

8

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

9

[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. 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.

10

Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation.

Men M, Jiang L, Wang H, Liu Y, Hu Z, He C, Feng Y. Men M, et al. Acta Otolaryngol. 2011 Sep;131(9):970-5. doi: 10.3109/00016489.2011.575794. Epub 2011 Apr 19. Acta Otolaryngol. 2011. PMID: 21504270

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