Wang Q - Search Results

1

[Advances in hereditary hearing loss caused by TMC1 mutations].

Wu K, Wang H, Wang Q. Wu K, et al. Among authors: wang h, wang q. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016 Mar;51(3):224-9. doi: 10.3760/cma.j.issn.1673-0860.2016.03.016. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016. PMID: 27033582 Chinese.

2

[A report on a large family with X-linked recessive nonsyndromic hereditary low frequency neuropathic hearing impairment].

Wang Q, Cao J, Yu L, Guo W, Yu N, Yang W, Gu R. Wang Q, et al. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2002 Aug;37(4):247-51. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2002. PMID: 12772406 Chinese.

3

[KCNQ4 gene mutations affected a pedigree with autosomal dominant hereditary hearing loss].

Wang Q, Cao J, Li N, Yang Y, Wang Q, Yu L, Han D, Yang W. Wang Q, et al. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2002 Oct;37(5):343-7. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2002. PMID: 12772453 Chinese.

4

[Inferior vestibular nerve impairment in auditory neuropathy].

Wu ZM, Zhou N, Zhang SZ, Wang QJ, Guo WW, Gu R, Yu LM, Yang WY, Han DY. Wu ZM, et al. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2004 Aug;39(8):486-8. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2004. PMID: 15563085 Chinese.

5

A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family.

Wang QJ, Li QZ, Rao SQ, Zhao YL, Yuan H, Yang WY, Han DY, Shen Y. Wang QJ, et al. Laryngoscope. 2006 Jun;116(6):944-50. doi: 10.1097/01.MLG.0000215285.53045.24. Laryngoscope. 2006. PMID: 16735904

6

[Clinical classification and relationship with conductive deafness of congenital middle ear malformations].

Yuan H, Wang QJ, Han DY. Yuan H, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005 Dec;40(12):893-5. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005. PMID: 16874955 Chinese.

7

[The characteristic of enlarged vestibular aqueducts syndrome in pure tone audiometry: low frequency air-bone gap].

Lan L, Wang Q, Chen Z, Ding H, Zhao J, Guo M, Yu L. Lan L, et al. Among authors: wang q. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Apr;21(7):309-11. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17580717 Chinese.

8

[The roles of connexin genes in sporadic hearing loss population].

Li QZ, Wang QJ, Chi FL, Li LN, Zhao YL, Yuan H, Han DY. Li QZ, et al. Zhonghua Yi Xue Za Zhi. 2007 Apr 24;87(16):1097-101. Zhonghua Yi Xue Za Zhi. 2007. PMID: 17672988 Chinese.

9

[Gene mapping for autosomal dominant nonsyndromic hearing loss DFNA11].

Yuan H, Han DY, Wang QJ, Zong L, Zhao YL. Yuan H, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Jun;42(6):422-7. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17702415 Chinese.

10

[Prenatal diagnosis for hereditary deaf families assisted by genetic testing].

Han B, Dai P, Qi QW, Wang LX, Wang Y, Bian XM, Wang QJ, Zhang X, Kang DY, Wang GJ, Han DY. Han B, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Sep;42(9):660-3. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18051563 Chinese.

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