Wang QJ - Search Results

1

Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome.

Wang L, Lin QF, Wang HY, Guan J, Lan L, Xie LY, Yu L, Yang J, Zhao C, Liang JL, Zhou HL, Yang HM, Xiong WP, Zhang QJ, Wang DY, Wang QJ. Wang L, et al. Among authors: wang hy, wang dy, wang qj. Chin Med J (Engl). 2017 Mar 20;130(6):703-709. doi: 10.4103/0366-6999.201600. Chin Med J (Engl). 2017. PMID: 28303854 Free PMC article.

2

[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.

3

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

4

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.

5

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

Yuan H, Wang QJ, Han DY. Yuan H, et al. Among authors: wang qj. 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.

6

[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. 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.

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. Among authors: wang qj. 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

GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.

Guo YF, Liu XW, Guan J, Han MK, Wang DY, Zhao YL, Rao SQ, Wang QJ. Guo YF, et al. Among authors: wang dy, wang qj. Acta Otolaryngol. 2008 Mar;128(3):297-303. doi: 10.1080/00016480701767382. Acta Otolaryngol. 2008. PMID: 18274916

9

[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.

10

[Correlation between phonetically balanced maximum and pure tone auditory threshold among 106 auditory neuropathy patients].

Lan L, Han DY, Shi W, Han MK, Liu Q, Ding HN, Chen ZH, Wang DY, Li SH, Guo ML, Rao SQ, Wang QJ. Lan L, et al. Among authors: wang dy, wang qj. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008 May;43(5):341-6. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008. PMID: 18717308 Chinese.

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