Han MY - Search Results

1

Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing.

Gao X, Zhu QY, Song YS, Wang GJ, Yuan YY, Xin F, Huang SS, Kang DY, Han MY, Guan LP, Zhang JG, Dai P. Gao X, et al. Among authors: han my. J Transl Med. 2013 Nov 9;11:284. doi: 10.1186/1479-5876-11-284. J Transl Med. 2013. PMID: 24206587 Free PMC article.

2

[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype].

Wang G, Yuan Y, Li R, Han M, Huang S, Kang D, Zhang X, Dong M, Dai P, Han D. Wang G, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011 May;25(10):445-8. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011. PMID: 21809555 Chinese.

3

[Prenatal genetic counseling and instruction for deaf families by genetic test].

Han MY, Huang SS, Wang GJ, Yuan YY, Kang DY, Zhang X, Dai P. Han MY, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011 Nov;46(11):909-13. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011. PMID: 22335977 Chinese.

4

[Prenatal genetic test and clinical guidance for 213 hereditary deaf families].

Han MY, Lu YP, Bian XM, Wang LX, Huang SS, Wang GJ, Wang Y, Kang DY, Zhang X, Dai P. Han MY, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Feb;47(2):127-31. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 22455811 Chinese.

5

Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China.

Yuan Y, Guo W, Tang J, Zhang G, Wang G, Han M, Zhang X, Yang S, He DZ, Dai P. Yuan Y, et al. PLoS One. 2012;7(11):e49984. doi: 10.1371/journal.pone.0049984. Epub 2012 Nov 21. PLoS One. 2012. PMID: 23185506 Free PMC article.

6

Sensorineural hearing loss caused by mutations in two alleles of both GJB2 and SLC26A4 genes.

Huang S, Han D, Wang G, Yuan Y, Song Y, Han M, Chen Z, Dai P. Huang S, et al. Int J Pediatr Otorhinolaryngol. 2013 Mar;77(3):379-83. doi: 10.1016/j.ijporl.2012.11.031. Epub 2012 Dec 21. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23266159

7

Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese family.

Gao X, Su Y, Guan LP, Yuan YY, Huang SS, Lu Y, Wang GJ, Han MY, Yu F, Song YS, Zhu QY, Wu J, Dai P. Gao X, et al. Among authors: han my. PLoS One. 2013 May 14;8(5):e63026. doi: 10.1371/journal.pone.0063026. Print 2013. PLoS One. 2013. PMID: 23690975 Free PMC article.

8

Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China.

Xin F, Yuan Y, Deng X, Han M, Wang G, Zhao J, Gao X, Liu J, Yu F, Han D, Dai P. Xin F, et al. J Transl Med. 2013 Dec 17;11:312. doi: 10.1186/1479-5876-11-312. J Transl Med. 2013. PMID: 24341454 Free PMC article.

9

Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation.

Zhu Y, Huang S, Kang D, Han M, Wang G, Yuan Y, Su Y, Yuan H, Zhai S, Dai P. Zhu Y, et al. BMC Genet. 2014 Feb 17;15:26. doi: 10.1186/1471-2156-15-26. BMC Genet. 2014. PMID: 24533451 Free PMC article.

10

A novel mutation in the TECTA gene in a Chinese family with autosomal dominant nonsyndromic hearing loss.

Su Y, Tang WX, Gao X, Yu F, Dai ZY, Zhao JD, Lu Y, Ji F, Huang SS, Yuan YY, Han MY, Song YS, Zhu YH, Kang DY, Han DY, Dai P. Su Y, et al. Among authors: han dy, han my. PLoS One. 2014 Feb 21;9(2):e89240. doi: 10.1371/journal.pone.0089240. eCollection 2014. PLoS One. 2014. PMID: 24586623 Free PMC article.

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