Zhang C - Search Results

1

Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics.

Shen Z, Zheng J, Chen B, Peng G, Zhang T, Gong S, Zhu Y, Zhang C, Li R, Yang L, Zhou J, Cai T, Jin L, Lu J, Guan MX. Shen Z, et al. Among authors: zhang c, zhang t. J Transl Med. 2011 Jan 4;9:4. doi: 10.1186/1479-5876-9-4. J Transl Med. 2011. PMID: 21205314 Free PMC article.

2

Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees.

Chen B, Sun D, Yang L, Zhang C, Yang A, Zhu Y, Zhao J, Chen Y, Guan M, Wang X, Li R, Tang X, Wang J, Tao Z, Lu J, Guan MX. Chen B, et al. Among authors: zhang c. Am J Med Genet A. 2008 May 15;146A(10):1248-58. doi: 10.1002/ajmg.a.32285. Am J Med Genet A. 2008. PMID: 18386806

3

[Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss in five Han Chinese pedigrees].

Zhang T, Chen BB, Zheng J, Gong SS, Zhang CQ, Lv JX, Guan MX. Zhang T, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):367-73. doi: 10.3760/cma.j.issn.1003-9406.2011.04.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21811972 Chinese.

4

[Characterization of two Chinese families with aminoglycoside-induced and nonsyndromic hearing loss both carrying a mitochondrial 12S rRNA 1494C>T mutation].

Gong SS, Chen BB, Peng GH, Zheng J, Zhang T, Zheng BJ, Fang F, Zhang CQ, Lv JX, Guan MX. Gong SS, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):382-7. doi: 10.3760/cma.j.issn.1003-9406.2012.04.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875491 Chinese.

5

[Genetic analysis of family constellation for cochlear implant recipients].

Zhang CQ, Chen BB, Huang JY, Sun DM, Chen YY, Xiang SJ, Guan MX. Zhang CQ, et al. Yi Chuan. 2008 Nov;30(11):1406-10. doi: 10.3724/sp.j.1005.2008.01406. Yi Chuan. 2008. PMID: 19073547 Chinese.

6

[Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment].

Zhang CQ, Chen BB, Chen YY, Liu XJ, Zheng J, Gao JJ, Huang SY, Nan BY, Zhang YY, Yu X, Guan MX. Zhang CQ, et al. Yi Chuan. 2013 Mar;35(3):352-8. doi: 10.3724/sp.j.1005.2013.00352. Yi Chuan. 2013. PMID: 23575541 Chinese.

7

[Analysis of genotype-phenotype correlation for GJB2 in 221 non-syndromic deafness probands and their pedigrees].

Yu X, Chen BB, Xiang HJ, Nan BY, Zheng J, Zhang CQ, Gao JJ, Zheng BJ, Chen YY, Guan MX. Yu X, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Dec;48(12):991-5. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013. PMID: 24506997 Chinese.

8

Genetic Polymorphisms and Susceptibility to Sudden Sensorineural Hearing Loss: A Systematic Review.

Cao Z, Gao J, Huang S, Xiang H, Zhang C, Zheng B, Zhan X, Chen R, Chen B. Cao Z, et al. Among authors: zhang c. Audiol Neurootol. 2019;24(1):8-19. doi: 10.1159/000497032. Epub 2019 Mar 14. Audiol Neurootol. 2019. PMID: 30870848

9

[Report of an infant with temporal bone Langerhans cell histiocytosis].

Zhang CQ, Chen BB, Yang L. Zhang CQ, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Jul;42(7):539. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17886688 Chinese. No abstract available.

10

[Peri-operative management on juvenile recurrent respiratory papillomatosis].

Nan BY, Chen BB, Zhang CQ. Nan BY, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Jun;47(6):454-7. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 22932135 Chinese.

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