Yang T - Search Results

1

A dominant variant in DMXL2 is linked to nonsyndromic hearing loss.

Chen DY, Liu XF, Lin XJ, Zhang D, Chai YC, Yu DH, Sun CL, Wang XL, Zhu WD, Chen Y, Sun LH, Wang XW, Shi FX, Huang ZW, Yang T, Wu H. Chen DY, et al. Among authors: yang t. Genet Med. 2017 May;19(5):553-558. doi: 10.1038/gim.2016.142. Epub 2016 Sep 22. Genet Med. 2017. PMID: 27657680 Free article.

2

Autosomal dominant nonsyndromic hearing impairment.

Van Laer L, McGuirt WT, Yang T, Smith RJ, Van Camp G. Van Laer L, et al. Among authors: yang t. Am J Med Genet. 1999 Sep 24;89(3):167-74. doi: 10.1002/(sici)1096-8628(19990924)89:3<167::aid-ajmg7>3.3.co;2-m. Am J Med Genet. 1999. PMID: 10704191 Review.

3

Genetic heterogeneity of deafness phenotypes linked to DFNA4.

Yang T, Pfister M, Blin N, Zenner HP, Pusch CM, Smith RJ. Yang T, et al. Am J Med Genet A. 2005 Nov 15;139(1):9-12. doi: 10.1002/ajmg.a.30989. Am J Med Genet A. 2005. PMID: 16222661

4

A novel splice site mutation in EYA4 causes DFNA10 hearing loss.

Hildebrand MS, Coman D, Yang T, Gardner RJ, Rose E, Smith RJ, Bahlo M, Dahl HH. Hildebrand MS, et al. Among authors: yang t. Am J Med Genet A. 2007 Jul 15;143A(14):1599-604. doi: 10.1002/ajmg.a.31860. Am J Med Genet A. 2007. PMID: 17568404

5

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.

6

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.

7

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

8

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

9

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.

10

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

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