Zong L - Search Results

1

Correlation analysis of genotypes, auditory function, and vestibular size in Chinese children with enlarged vestibular aqueduct syndrome.

Zhao FF, Lan L, Wang DY, Han B, Qi Y, Zhao Y, Zong L, Li Q, Wang QJ. Zhao FF, et al. Among authors: zong l. Acta Otolaryngol. 2013 Dec;133(12):1242-9. doi: 10.3109/00016489.2013.822555. Acta Otolaryngol. 2013. PMID: 24245694

2

The large Chinese family with Y-linked hearing loss revisited: clinical investigation.

Wang QJ, Rao SQ, Zhao YL, Liu QJ, Zong L, Han MK, Han DY, Yang WY. Wang QJ, et al. Among authors: zong l. Acta Otolaryngol. 2009 Jun;129(6):638-43. doi: 10.1080/00016480802216347. Acta Otolaryngol. 2009. PMID: 18720061

3

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. Among authors: zong l. 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.

4

Unilateral auditory neuropathy spectrum disorder.

Zhang QJ, Lan L, Shi W, Wang DY, Qi Y, Zong L, Li Q, Wang H, Ding HN, Li N, Han B, Wang QJ. Zhang QJ, et al. Among authors: zong l. Acta Otolaryngol. 2012 Jan;132(1):72-9. doi: 10.3109/00016489.2011.629630. Epub 2011 Nov 10. Acta Otolaryngol. 2012. PMID: 22073929

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: zong l. 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

[Clinical analysis of in-patients with large vestibular aqueduct syndrome].

Wang D, Zhao Y, Zhao F, Zong L, Han B, Lan L, Zhang Q, Qi Y, Wang Q. Wang D, et al. Among authors: zong l. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Oct;27(19):1063-7. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013. PMID: 24417164 Chinese.

7

Comparative study of mutation spectrums of MT-RNR1 m.1555A>G, GJB2, and SLC26A4 between familial and sporadic patients with nonsyndromic sensorineural hearing loss in Chinese Han.

Li Q, Ji Y, Han B, Zong L, Lan L, Zhao Y, Wang H, Wang D, Wang Q. Li Q, et al. Among authors: zong l. Chin Med J (Engl). 2014;127(18):3233-7. Chin Med J (Engl). 2014. PMID: 25266519

8

Identification of a novel mutation of PJVK in the Chinese non-syndromic hearing loss population with low prevalence of the PJVK mutations.

Zhang QJ, Lan L, Li N, Qi Y, Zong L, Shi W, Yu L, Wang H, Yang J, Xie LY, Zhao F, Wang DY, Han B, Wang QJ. Zhang QJ, et al. Among authors: zong l. Acta Otolaryngol. 2015 Mar;135(3):211-6. doi: 10.3109/00016489.2014.985799. Epub 2015 Jan 28. Acta Otolaryngol. 2015. PMID: 25631766

9

Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype-phenotype review for DFNA11.

Li L, Yuan H, Wang H, Guan J, Lan L, Wang D, Zong L, Liu Q, Han B, Huang D, Wang Q. Li L, et al. Among authors: zong l. Acta Otolaryngol. 2018 May;138(5):463-470. doi: 10.1080/00016489.2017.1397743. Epub 2018 Feb 5. Acta Otolaryngol. 2018. PMID: 29400105

10

A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China.

Wang QJ, Zhao YL, Rao SQ, Guo YF, Yuan H, Zong L, Guan J, Xu BC, Wang DY, Han MK, Lan L, Zhai SQ, Shen Y. Wang QJ, et al. Among authors: zong l. Clin Genet. 2007 Sep;72(3):245-54. doi: 10.1111/j.1399-0004.2007.00862.x. Clin Genet. 2007. PMID: 17718863

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