Yang T - Search Results

1

[Genetic research of age-related hearing impairment].

Luo HJ, Yang T, Wu H. Luo HJ, et al. Among authors: yang t. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Jan;48(1):78-81. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013. PMID: 23656826 Review. Chinese. No abstract available.

2

Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome.

Yang T, Gurrola JG 2nd, Wu H, Chiu SM, Wangemann P, Snyder PM, Smith RJ. Yang T, et al. Am J Hum Genet. 2009 May;84(5):651-7. doi: 10.1016/j.ajhg.2009.04.014. Epub 2009 May 7. Am J Hum Genet. 2009. PMID: 19426954 Free PMC article.

3

Genotype-phenotype correlation of two prevalent GJB2 mutations in Chinese newborn infants ascertained from the Universal Newborn Hearing Screening Program.

Ma Y, Yang T, Li Y, Tao Z, Huang Z, Li X, Chai Y, Ouyang Z, Shen X, Wu H. Ma Y, et al. Among authors: yang t. Am J Med Genet A. 2010 Nov;152A(11):2912-5. doi: 10.1002/ajmg.a.33698. Am J Med Genet A. 2010. PMID: 20954238 No abstract available.

4

Screening for delayed-onset hearing loss in preschool children who previously passed the newborn hearing screening.

Lü J, Huang Z, Yang T, Li Y, Mei L, Xiang M, Chai Y, Li X, Li L, Yao G, Wang Y, Shen X, Wu H. Lü J, et al. Among authors: yang t. Int J Pediatr Otorhinolaryngol. 2011 Aug;75(8):1045-9. doi: 10.1016/j.ijporl.2011.05.022. Epub 2011 Jun 25. Int J Pediatr Otorhinolaryngol. 2011. PMID: 21705096

5

Novel mutations in ATP6V0A4 are associated with atypical progressive sensorineural hearing loss in a Chinese patient with distal renal tubular acidosis.

Li X, Chai Y, Tao Z, Li L, Huang Z, Li Y, Wu H, Yang T. Li X, et al. Among authors: yang t. Int J Pediatr Otorhinolaryngol. 2012 Jan;76(1):152-4. doi: 10.1016/j.ijporl.2011.10.017. Epub 2011 Nov 16. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22093743

6

The p.V37I exclusive genotype of GJB2: a genetic risk-indicator of postnatal permanent childhood hearing impairment.

Li L, Lu J, Tao Z, Huang Q, Chai Y, Li X, Huang Z, Li Y, Xiang M, Yang J, Yao G, Wang Y, Yang T, Wu H. Li L, et al. Among authors: yang t, yang j. PLoS One. 2012;7(5):e36621. doi: 10.1371/journal.pone.0036621. Epub 2012 May 4. PLoS One. 2012. PMID: 22574200 Free PMC article.

7

The effect of GJB2 and SLC26A4 gene mutations on rehabilitative outcomes in pediatric cochlear implant patients.

Yan YJ, Li Y, Yang T, Huang Q, Wu H. Yan YJ, et al. Among authors: yang t. Eur Arch Otorhinolaryngol. 2013 Nov;270(11):2865-70. doi: 10.1007/s00405-012-2330-y. Epub 2013 Jan 8. Eur Arch Otorhinolaryngol. 2013. PMID: 23296490

8

[Prenatal screening and diagnosis of genetic deafness by microarray].

Sun LH, Li L, Wang XW, Zhu YZ, Chai YC, Li XH, Wu H, Yang T. Sun LH, et al. Among authors: yang t. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Dec;47(12):991-5. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 23328038 Chinese.

9

Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing.

Yang T, Wei X, Chai Y, Li L, Wu H. Yang T, et al. Orphanet J Rare Dis. 2013 Jun 14;8:85. doi: 10.1186/1750-1172-8-85. Orphanet J Rare Dis. 2013. PMID: 23767834 Free PMC article.

10

Molecular etiology of hearing impairment associated with nonsyndromic enlarged vestibular aqueduct in East China.

Chai Y, Huang Z, Tao Z, Li X, Li L, Li Y, Wu H, Yang T. Chai Y, et al. Among authors: yang t. Am J Med Genet A. 2013 Sep;161A(9):2226-33. doi: 10.1002/ajmg.a.36068. Epub 2013 Aug 5. Am J Med Genet A. 2013. PMID: 23918157

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