Zhu Q - Search Results

1

A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2.

Huang B, Liu Y, Gao X, Xu J, Dai P, Zhu Q, Yuan Y. Huang B, et al. Among authors: zhu q. BMC Med Genet. 2017 Mar 24;18(1):36. doi: 10.1186/s12881-017-0396-5. BMC Med Genet. 2017. PMID: 28340560 Free PMC article.

2

[Patients suffered from enlarged vestibular aqueduct syndrome in Chifeng deaf and dumb school detected by Pendred's syndrome gene hot spot mutation screening].

Dai P, Zhu XH, Yuan YY, Zhu QW, Teng GC, Zhang X, Liu LX, Wang JL, Feng B, Zhai SQ, Kang DY, Liu X, Huang DL. Dai P, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2006 Jul;41(7):497-500. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2006. PMID: 17007371 Chinese.

3

The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss.

Han D, Dai P, Zhu Q, Liu X, Huang D, Yuan Y, Yuan H, Wang X, Qian Y, Young WY, Guan MX. Han D, et al. Among authors: zhu q. Biochem Biophys Res Commun. 2007 Jun 1;357(2):554-60. doi: 10.1016/j.bbrc.2007.03.199. Epub 2007 Apr 9. Biochem Biophys Res Commun. 2007. PMID: 17434445

4

[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: zhu q. 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.

5

[Molecular etiology of 573 patients with nonsyndromic hearing loss in 5 provinces of northwest region of China].

Zhu Q, Liu X, Han D, Kang D, Zhang X, Jin Z, Li M, Dai P. Zhu Q, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 May;21(10):460-2. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 17650818 Chinese.

6

[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.

7

[Sequencing of SLC26A4 exons 7 and 8 and hot spot mutation analysis in 1552 moderate to profound sensorineural hearing loss patients in China].

Dai P, Yuan YY, Kang DY, Li Q, Zhu QW, Zhang X, Liu LX, Liu X, Huang DL. Dai P, et al. Among authors: zhu qw. Zhonghua Yi Xue Za Zhi. 2007 Sep 25;87(36):2521-5. Zhonghua Yi Xue Za Zhi. 2007. PMID: 18067822 Chinese.

8

[Mutation of GJB2 gene in nonsyndromic hearing impairment patients: analysis of 1190 cases].

Yu F, Han DY, Dai P, Kang DY, Zhang X, Liu X, Zhu QW, Yuan YY, Sun Q, Xue DD, Li M, Liu J, Yuan HJ, Yang WY. Yu F, et al. Among authors: zhu qw. Zhonghua Yi Xue Za Zhi. 2007 Oct 30;87(40):2814-9. Zhonghua Yi Xue Za Zhi. 2007. PMID: 18167282 Chinese.

9

[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. Among authors: zhu qw. Zhonghua Yi Xue Za Zhi. 2007 Nov 13;87(42):2977-81. Zhonghua Yi Xue Za Zhi. 2007. PMID: 18261328 Chinese.

10

[Frequency of SLC26A4 IVS7-2A > G mutation in patients with severe to profound hearing loss from different area and ethnic group in China].

Li Q, Dai P, Huang DL, Yuan YY, Zhu QW, Han B, Liu X, Yu F, Kang DY, Zhang X, Xue DD, Jin ZC. Li Q, et al. Among authors: zhu qw. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 Dec;42(12):893-7. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007. PMID: 18335745 Chinese.

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