Chai YC - Search Results

1

Mutation analysis of seven consanguineous Uyghur families with non-syndromic deafness.

Wang ZT, Chen Y, Chen DY, Chai YC, Pang XH, Sun LH, Wang XW, Yang T, Wu H. Wang ZT, et al. Among authors: chai yc. Int J Pediatr Otorhinolaryngol. 2014 Sep;78(9):1513-6. doi: 10.1016/j.ijporl.2014.06.023. Epub 2014 Jun 23. Int J Pediatr Otorhinolaryngol. 2014. PMID: 25015771

2

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. 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.

3

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. 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

4

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. 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

5

Double heterozygous mutations of MITF and PAX3 result in Waardenburg syndrome with increased penetrance in pigmentary defects.

Yang T, Li X, Huang Q, Li L, Chai Y, Sun L, Wang X, Zhu Y, Wang Z, Huang Z, Li Y, Wu H. Yang T, et al. Clin Genet. 2013 Jan;83(1):78-82. doi: 10.1111/j.1399-0004.2012.01853.x. Epub 2012 Mar 5. Clin Genet. 2013. PMID: 22320238

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. 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

[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: chai yc. 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.

8

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.

9

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. 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

10

Clinical characterization of a novel COCH mutation G87V in a Chinese DFNA9 family.

Chen DY, Chai YC, Yang T, Wu H. Chen DY, et al. Among authors: chai yc. Int J Pediatr Otorhinolaryngol. 2013 Oct;77(10):1711-5. doi: 10.1016/j.ijporl.2013.07.031. Epub 2013 Aug 9. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23993205

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