Wang D - Search Results

1

Novel recessive PDZD7 biallelic mutations in two Chinese families with non-syndromic hearing loss.

Guan J, Wang H, Lan L, Wang L, Yang J, Xie L, Yin Z, Xiong W, Zhao L, Wang D, Wang Q. Guan J, et al. Among authors: wang h, wang l, wang d, wang q. Am J Med Genet A. 2018 Jan;176(1):99-106. doi: 10.1002/ajmg.a.38477. Epub 2017 Oct 19. Am J Med Genet A. 2018. PMID: 29048736 Free PMC article.

2

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. Acta Otolaryngol. 2008 Mar;128(3):297-303. doi: 10.1080/00016480701767382. Acta Otolaryngol. 2008. PMID: 18274916

3

[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. 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.

4

[Audiological characteristics of young children with otitis media with effusion].

Wang QJ, Shi W, Lan L, Wang DY, Zhang YM. Wang QJ, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008 Dec;43(12):891-5. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008. PMID: 19141237 Chinese.

5

[Audiological and genetic studies on 130 infants with hearing loss].

Wang DY, Wang QJ, Lan L, Shi W, Zhao C, Hui PL, Rao SQ, Han DY. Wang DY, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009 Mar;44(3):177-81. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009. PMID: 19558853 Chinese.

6

[Evaluation of deaf-mute patients with sensitive deafness gene screening in Shandong province].

Ji YB, Han DY, Wang DY, Zhou Y, Zhao C, Wang H, Lan L, Wang QJ. Ji YB, et al. Zhonghua Yi Xue Za Zhi. 2009 Sep 29;89(36):2531-5. Zhonghua Yi Xue Za Zhi. 2009. PMID: 20137612 Chinese.

7

Identification of two novel mutations, c.232T>C and c.2006A>T, in SLC26A4 in a Chinese family associated with enlarged vestibular aqueduct.

Guo YF, Wang YL, Xu BC, Liu XW, Zhu YM, Zhao FF, Ji YB, Zhou Y, Li JQ, Li Q, Wang DY, Wang QJ. Guo YF, et al. Int J Pediatr Otorhinolaryngol. 2010 Jul;74(7):831-5. doi: 10.1016/j.ijporl.2010.04.005. Epub 2010 May 18. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20483489

8

Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy.

Wang DY, Wang YC, Weil D, Zhao YL, Rao SQ, Zong L, Ji YB, Liu Q, Li JQ, Yang HM, Shen Y, Benedict-Alderfer C, Zheng QY, Petit C, Wang QJ. Wang DY, et al. Among authors: wang yc, wang qj. BMC Med Genet. 2010 May 26;11:79. doi: 10.1186/1471-2350-11-79. BMC Med Genet. 2010. PMID: 20504331 Free PMC article.

9

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.

Ji YB, Han DY, Lan L, Wang DY, Zong L, Zhao FF, Liu Q, Benedict-Alderfer C, Zheng QY, Wang QJ. Ji YB, et al. Acta Otolaryngol. 2011 Feb;131(2):124-9. doi: 10.3109/00016489.2010.483479. Epub 2010 Dec 16. Acta Otolaryngol. 2011. PMID: 21162657 Free PMC article.

10

Phenotype-genotype correlation in 295 Chinese deaf subjects with biallelic causative mutations in the GJB2 gene.

Zhao FF, Ji YB, Wang DY, Lan L, Han MK, Li Q, Zhao Y, Rao S, Han D, Wang QJ. Zhao FF, et al. Among authors: wang dy, wang qj. Genet Test Mol Biomarkers. 2011 Sep;15(9):619-25. doi: 10.1089/gtmb.2010.0192. Epub 2011 Apr 13. Genet Test Mol Biomarkers. 2011. PMID: 21488715

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