Qi Y - Search Results

1

Mutation analysis of potassium channel genes KCNQ1 and KCNH2 in patients with long QT syndrome.

Liu W, Hu D, Li C, Li P, Li Y, Li Z, Li L, Qin X, Dong W, Qi Y, Chen S, Wang Q. Liu W, et al. Among authors: qi y. Chin Med J (Engl). 2003 Sep;116(9):1333-5. Chin Med J (Engl). 2003. PMID: 14527360

2

[Association between pre-excitation syndrome and 7q3 D7S505 pseudonym gene].

Liu W, Liu G, Hu D, Qi Y, Shan Z, Luo L, Zhang M, Wang L, Yi J. Liu W, et al. Among authors: qi y. Zhonghua Yi Xue Za Zhi. 2002 Jun 25;82(12):820-3. Zhonghua Yi Xue Za Zhi. 2002. PMID: 12126529 Chinese.

3

Detection of A3243G point mutation in mitochondrial DNA from 10 cases of MELAS.

Wang Z, Liu S, Yang Y, Yuan Y, Wu L, Qi Y, Chen Q. Wang Z, et al. Among authors: qi y. Chin Med J (Engl). 2002 Jul;115(7):995-7. Chin Med J (Engl). 2002. PMID: 12150728

4

KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.

Liu W, Yang J, Hu D, Kang C, Li C, Zhang S, Li P, Chen Z, Qin X, Ying K, Li Y, Li Y, Li Z, Cheng X, Li L, Qi Y, Chen S, Wang Q. Liu W, et al. Among authors: qi y. Hum Mutat. 2002 Dec;20(6):475-6. doi: 10.1002/humu.9085. Hum Mutat. 2002. PMID: 12442276 Free PMC article.

5

Familial Wolff-Parkinson-White syndrome is linked to the loci on chromosome 7q3.

Liu W, Liu G, Hu D, Qi Y, Shan Z, Yang D, Liu D, Wang Y. Liu W, et al. Among authors: qi y. Chin Med J (Engl). 2002 Nov;115(11):1733-5. Chin Med J (Engl). 2002. PMID: 12609097

6

[Heterozygous mutation in KCNQ1 cause Jervell and Lange-Nielsen syndrome].

Liu WL, Hu DY, Li P, Li CL, Qin XG, Li YT, Li L, Li ZM, Dong W, Qi Y, Wang Q. Liu WL, et al. Among authors: qi y. Zhonghua Xin Xue Guan Bing Za Zhi. 2005 Jan;33(1):41-4. Zhonghua Xin Xue Guan Bing Za Zhi. 2005. PMID: 15924777 Chinese.

7

Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.

Yang YL, Sun F, Zhang Y, Qian N, Yuan Y, Wang ZX, Qi Y, Xiao JX, Wang XY, Qi ZY, Zhang YH, Jiang YW, Bao XH, Qin J, Wu XR. Yang YL, et al. Among authors: qi y, qi zy. Chin Med J (Engl). 2006 Mar 5;119(5):373-7. Chin Med J (Engl). 2006. PMID: 16542579

8

[Novel mutations of potassium channel KCNQ1 S145L and KCNH2 Y475C genes in Chinese pedigrees of long QT syndrome].

Liu WL, Hu DY, Li P, Li CL, Qin XG, Li YT, Li L, Li ZM, Dong W, Qi Y, Wang Q. Liu WL, et al. Among authors: qi y. Zhonghua Nei Ke Za Zhi. 2006 Jun;45(6):463-6. Zhonghua Nei Ke Za Zhi. 2006. PMID: 16831322 Chinese.

9

[Molecular genetic analysis of mitochondrial DNA C1494T mutation in non-syndromic hearing loss of Chinese population].

Tian G, Liu YH, Ma YN, Li YJ, Zhang Y, Niu SL, Xu YE, Pei P, Wang ST, Bu DF, Du BR, Zhou X, Ke XM, Qi Y. Tian G, et al. Among authors: qi y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Aug;24(4):464-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17680545 Chinese.

10

[Analysis of the GABRG2 gene mutation in a Chinese family with generalized epilepsy with febrile seizures plus].

Sun H, Zhang Y, Liu X, Ma X, Wu H, Xu K, Qi Y, Wu X. Sun H, et al. Among authors: qi y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):611-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065515 Chinese.

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