Wang QJ - Search Results

1

[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. Among authors: wang qj. Zhonghua Yi Xue Za Zhi. 2007 Apr 24;87(16):1097-101. Zhonghua Yi Xue Za Zhi. 2007. PMID: 17672988 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

Familial auditory neuropathy.

Wang Q, Gu R, Han D, Yang W. Wang Q, et al. Laryngoscope. 2003 Sep;113(9):1623-9. doi: 10.1097/00005537-200309000-00041. Laryngoscope. 2003. PMID: 12972945

5

[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. Among authors: wang qj. 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.

6

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.

Wang Q, Li R, Zhao H, Peters JL, Liu Q, Yang L, Han D, Greinwald JH Jr, Young WY, Guan MX. Wang Q, et al. Am J Med Genet A. 2005 Feb 15;133A(1):27-30. doi: 10.1002/ajmg.a.30424. Am J Med Genet A. 2005. PMID: 15637703 Free PMC article.

7

[Genetic analysis in a Chinese deaf-mute family with X linked recessive inheritance].

Wang QJ, Yang WY, Wu ZM, Li QZ, Guo WW, Qiu CY. Wang QJ, et al. Yi Chuan. 2004 Sep;26(5):579-83. Yi Chuan. 2004. PMID: 15640065 Chinese.

8

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.

Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH Jr, Guan MX. Young WY, et al. Biochem Biophys Res Commun. 2005 Mar 25;328(4):1244-51. doi: 10.1016/j.bbrc.2005.01.085. Biochem Biophys Res Commun. 2005. PMID: 15708009

9

Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss.

Zhao H, Young WY, Yan Q, Li R, Cao J, Wang Q, Li X, Peters JL, Han D, Guan MX. Zhao H, et al. Nucleic Acids Res. 2005 Feb 18;33(3):1132-9. doi: 10.1093/nar/gki262. Print 2005. Nucleic Acids Res. 2005. PMID: 15722487 Free PMC article.

10

Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.

Zhao L, Wang Q, Qian Y, Li R, Cao J, Hart LC, Zhai S, Han D, Young WY, Guan MX. Zhao L, et al. Biochem Biophys Res Commun. 2005 Oct 28;336(3):967-73. doi: 10.1016/j.bbrc.2005.08.199. Biochem Biophys Res Commun. 2005. PMID: 16168391

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