Wang QJ - Search Results

1

[Studies of the strategy for newborn gene screening].

Wang QJ, Zhao YL, Lan L, Zhao C, Han MK, Han DY. Wang QJ, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Nov;42(11):809-13. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18300440 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

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family.

Zhao H, Li R, Wang Q, Yan Q, Deng JH, Han D, Bai Y, Young WY, Guan MX. Zhao H, et al. Am J Hum Genet. 2004 Jan;74(1):139-52. doi: 10.1086/381133. Epub 2003 Dec 12. Am J Hum Genet. 2004. PMID: 14681830 Free PMC article.

6

[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.

7

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.

8

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.

9

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

10

Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.

Wang Q, Li QZ, Han D, Zhao Y, Zhao L, Qian Y, Yuan H, Li R, Zhai S, Young WY, Guan MX. Wang Q, et al. Biochem Biophys Res Commun. 2006 Feb 10;340(2):583-8. doi: 10.1016/j.bbrc.2005.12.045. Epub 2005 Dec 19. Biochem Biophys Res Commun. 2006. PMID: 16380089

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