Mei LY - Search Results

1

[Validation and analysis of Goldengate high-throughput deafness gene chip in detecting the patients with enlarged vestibular aqueduct syndrome].

Wu H, Jiang L, Liu C, Liu YL, Long MQ, Mei LY, He CF, Cai XZ, Chen HS, Feng Y. Wu H, et al. Among authors: mei ly. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2021 Feb 3;56(2):138-143. doi: 10.3760/cma.j.cn115330-20200302-00150. Online ahead of print. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2021. PMID: 33548943 Chinese.

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. 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

[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.

4

[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.

5

[Surgery of ventilation tube insertion in the middle ear and the external auditory canal for chronic secretory otitis media in children].

Mei LY, Feng Y, Liu HB, Cai XZ. Mei LY, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2008 Apr;10(2):155-7. Zhongguo Dang Dai Er Ke Za Zhi. 2008. PMID: 18433535 Chinese.

6

[Evaluation test and masking therapy of subjective tinnitus].

Zhang HL, Feng Y, Mei LY, Wen Y. Zhang HL, et al. Among authors: mei ly. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009 Aug;44(8):636-40. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009. PMID: 19961770 Chinese.

7

[Screening and identification interaction proteins of connexin 30].

He DH, Feng Y, Mei LY, He CF. He DH, et al. Among authors: mei ly. 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

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. 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

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