Wang G - Search Results

1

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. Among authors: wang g. PLoS One. 2012;7(11):e49984. doi: 10.1371/journal.pone.0049984. Epub 2012 Nov 21. PLoS One. 2012. PMID: 23185506 Free PMC article.

2

[GJB6 gene mutation analysis in Chinese nonsyndromic deaf population].

Yuan Y, Huang D, Dai P, Zhu Q, Liu X, Wang G, Li Q, Wu B. Yuan Y, et al. Among authors: wang g. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Jan;21(1):3-6. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17438853 Chinese.

3

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population.

Dai P, Yu F, Han B, Yuan Y, Li Q, Wang G, Liu X, He J, Huang D, Kang D, Zhang X, Yuan H, Schmitt E, Han D, Wong LJ. Dai P, et al. Among authors: wang g. Genet Med. 2007 May;9(5):283-9. doi: 10.1097/gim.0b013e31804d2371. Genet Med. 2007. PMID: 17505205 Free article.

4

[Genetic counseling and intervention for families with deaf-mute patients based on genetic testing: analysis of 5 families].

Dai P, Han B, Yuan YY, Jin ZC, Wang Y, Xiang Y, Yu F, Liu X, Wang GJ, Kang DY, Zhang X, Li M, Zhai SQ, Huang DL, Han DY. Dai P, et al. Zhonghua Yi Xue Za Zhi. 2007 Apr 24;87(16):1088-92. Zhonghua Yi Xue Za Zhi. 2007. PMID: 17672986 Chinese.

5

[Genetic counseling and instruction for deaf couples directed by genetic testing].

Han B, Dai P, Wang GJ, Kang DY, Zhang X, Yuan YY, Zhu QW, Jin ZC, Li M, Zhai SQ, Huang DL, Han DY. Han B, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Jul;42(7):499-503. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17886676 Chinese.

6

[Prenatal diagnosis for hereditary deaf families assisted by genetic testing].

Han B, Dai P, Qi QW, Wang LX, Wang Y, Bian XM, Wang QJ, Zhang X, Kang DY, Wang GJ, Han DY. Han B, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Sep;42(9):660-3. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18051563 Chinese.

7

[Prevalence of GJB2 mutations in Uigur and Han ethnic populations with deafness in Xinjiang region of China].

Li Q, Dai P, Huang DL, Zhang J, Wang GJ, Zhu QW, Liu X, Han DY. Li Q, et al. Zhonghua Yi Xue Za Zhi. 2007 Nov 13;87(42):2977-81. Zhonghua Yi Xue Za Zhi. 2007. PMID: 18261328 Chinese.

8

[Features of nationwide distribution and frequency of a common gap junction beta-2 gene mutation in China].

Dai P, Yu F, Han B, Wu H, Yuan YY, Li Q, Wang GJ, Liu X, He J, Huang DL, Kang DY, Zhang X, Yuan HJ, Leejun CW, Han DY. Dai P, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Nov;42(11):804-8. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18300439 Chinese.

9

[Mutation screening of MITF gene in patients with Waardenburg syndrome type 2].

Chen J, Yang SZ, Liu J, Han B, Wang GJ, Zhang X, Kang DY, Dai P, Young WY, Yuan HJ. Chen J, et al. Yi Chuan. 2008 Apr;30(4):433-8. doi: 10.3724/sp.j.1005.2008.00433. Yi Chuan. 2008. PMID: 18424413 Chinese.

10

Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss.

Chen J, Yuan H, Lu J, Liu X, Wang G, Zhu Y, Cheng J, Wang X, Han B, Yang L, Yang S, Yang A, Sun Q, Kang D, Zhang X, Dai P, Zhai S, Han D, Young WY, Guan MX. Chen J, et al. Among authors: wang x, wang g. Mitochondrion. 2008 Sep;8(4):285-92. doi: 10.1016/j.mito.2008.05.002. Epub 2008 May 23. Mitochondrion. 2008. PMID: 18639500

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