Wang Q - Search Results

1

Human Y chromosome base-substitution mutation rate measured by direct sequencing in a deep-rooting pedigree.

Xue Y, Wang Q, Long Q, Ng BL, Swerdlow H, Burton J, Skuce C, Taylor R, Abdellah Z, Zhao Y; Asan; MacArthur DG, Quail MA, Carter NP, Yang H, Tyler-Smith C. Xue Y, et al. Among authors: wang q. Curr Biol. 2009 Sep 15;19(17):1453-7. doi: 10.1016/j.cub.2009.07.032. Epub 2009 Aug 27. Curr Biol. 2009. PMID: 19716302 Free PMC article.

2

Genetic basis of Y-linked hearing impairment.

Wang Q, Xue Y, Zhang Y, Long Q, Asan, Yang F, Turner DJ, Fitzgerald T, Ng BL, Zhao Y, Chen Y, Liu Q, Yang W, Han D, Quail MA, Swerdlow H, Burton J, Fahey C, Ning Z, Hurles ME, Carter NP, Yang H, Tyler-Smith C. Wang Q, et al. Am J Hum Genet. 2013 Feb 7;92(2):301-6. doi: 10.1016/j.ajhg.2012.12.015. Epub 2013 Jan 24. Am J Hum Genet. 2013. PMID: 23352258 Free PMC article.

3

Improving global and regional resolution of male lineage differentiation by simple single-copy Y-chromosomal short tandem repeat polymorphisms.

Vermeulen M, Wollstein A, van der Gaag K, Lao O, Xue Y, Wang Q, Roewer L, Knoblauch H, Tyler-Smith C, de Knijff P, Kayser M. Vermeulen M, et al. Among authors: wang q. Forensic Sci Int Genet. 2009 Sep;3(4):205-13. doi: 10.1016/j.fsigen.2009.01.009. Epub 2009 Feb 23. Forensic Sci Int Genet. 2009. PMID: 19647704 Free PMC article.

4

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

5

Newborn genetic screening for high risk deafness-associated mutations with a new Tetra-primer ARMS PCR kit.

Han B, Zong L, Li Q, Zhang Z, Wang D, Lan L, Zhang J, Zhao Y, Wang Q. Han B, et al. Among authors: wang d, wang q. Int J Pediatr Otorhinolaryngol. 2013 Sep;77(9):1440-5. doi: 10.1016/j.ijporl.2013.05.040. Epub 2013 Jun 29. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23815884

6

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

7

[Mitochondrial DNA A1555G mutation analysis in 802 nonsyndromic hearing impairment patients].

Liu XW, Guo YF, Han DY, Zhao YL, Lan L, Zhao C, Wang QJ. Liu XW, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Oct;42(10):739-42. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18229583 Chinese.

8

[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.

9

Analysis of a large-scale screening of mitochondrial DNA m.1555A>G mutation in 2417 deaf-mute students in northwest of China.

Guo YF, Liu XW, Xu BC, Zhu YM, Wang YL, Zhao FF, Wang DY, Zhao YL, Ji YB, Wang QJ. Guo YF, et al. Genet Test Mol Biomarkers. 2010 Aug;14(4):527-31. doi: 10.1089/gtmb.2010.0020. Genet Test Mol Biomarkers. 2010. PMID: 20662562

10

[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.

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