Guo XM - Search Results

1

[Analysis of GUCA1B,GNGT1 and RGS9 genes in patients with retinitis pigmentosa].

Zhang QJ, Li W, Xiao XS, Li SQ, Guo XM. Zhang QJ, et al. Among authors: guo xm. Yi Chuan. 2002 Jan;24(1):19-21. Yi Chuan. 2002. PMID: 15901556 Chinese.

2

Mutations in RPGR and RP2 of Chinese patients with X-linked retinitis pigmentosa.

Ji Y, Wang J, Xiao X, Li S, Guo X, Zhang Q. Ji Y, et al. Curr Eye Res. 2010 Jan;35(1):73-9. doi: 10.3109/02713680903395299. Curr Eye Res. 2010. PMID: 20021257

3

[The SNPs analysis of encoding sequence of interacting factor gene in Chinese population].

Li J, Zhang QJ, Xiao XS, Li JZ, Zhang FS, Li SQ, Li W, Li T, Jia XY, Guo L, Guo XM. Li J, et al. Among authors: guo xm, guo l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Oct;20(5):454-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 14556208 Chinese.

4

[Variations of the zinc finger protein 161 gene in Chinese with or without high myopia].

Wang GB, Zhang QJ, Xiao XS, Li JZ, Zhang FS, Li SQ, Li W, Li T, Jia XY, Guo L, Guo XM. Wang GB, et al. Among authors: guo xm, guo l. Yi Chuan. 2004 Mar;26(2):155-9. Yi Chuan. 2004. PMID: 15639979 Chinese.

5

[Clinical features and the mutation of Leber's hereditary optic neuropathy in Chinese patients].

Wang Y, Guo XM, Jia XY, Li SQ, Xiao XS, Guo L, Zhang QJ. Wang Y, et al. Among authors: guo xm, guo l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):334-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15952130 Chinese.

6

[Variation of the peripherin gene in Chinese with or without high myopia].

Li J, Zhang QJ, Fu R, Xiao XS, Li JZ, Zhang FS, Li SQ, Li W, Li T, Jia XY, Guo L, Guo XM. Li J, et al. Among authors: guo xm, guo l. Yi Chuan. 2002 Sep;24(5):523-6. Yi Chuan. 2002. PMID: 16135441 Chinese.

7

Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.

Zhang Q, Guo X, Xiao X, Yi J, Jia X, Hejtmancik JF. Zhang Q, et al. Mol Vis. 2004 Nov 17;10:890-900. Mol Vis. 2004. PMID: 15570218 Free article.

8

A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.

Zhang Q, Guo X, Xiao X, Jia X, Li S, Hejtmancik JF. Zhang Q, et al. Mol Vis. 2005 Jul 22;11:554-60. Mol Vis. 2005. PMID: 16052171 Free article.

9

CSNB1 in Chinese families associated with novel mutations in NYX.

Xiao X, Jia X, Guo X, Li S, Yang Z, Zhang Q. Xiao X, et al. J Hum Genet. 2006;51(7):634-40. doi: 10.1007/s10038-006-0406-5. Epub 2006 May 3. J Hum Genet. 2006. PMID: 16670814

10

Novel mutations of the PAX6 gene identified in Chinese patients with aniridia.

Wang P, Guo X, Jia X, Li S, Xiao X, Zhang Q. Wang P, et al. Mol Vis. 2006 Jun 7;12:644-8. Mol Vis. 2006. PMID: 16785853 Free article.

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