Jia XY - Search Results

1

[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: jia xy. 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.

2

[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: jia xy. 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.

3

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.

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: jia xy. Yi Chuan. 2004 Mar;26(2):155-9. Yi Chuan. 2004. PMID: 15639979 Chinese.

5

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.

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: jia xy. Yi Chuan. 2002 Sep;24(5):523-6. Yi Chuan. 2002. PMID: 16135441 Chinese.

7

Linkage analysis of two families with X-linked recessive congenital motor nystagmus.

Guo X, Li S, Jia X, Xiao X, Wang P, Zhang Q. Guo X, et al. J Hum Genet. 2006;51(1):76-80. doi: 10.1007/s10038-005-0316-y. Epub 2005 Oct 21. J Hum Genet. 2006. PMID: 16240070

8

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

9

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.

10

Cataracts, ataxia, short stature, and mental retardation in a Chinese family mapped to Xpter-q13.1.

Guo X, Shen H, Xiao X, Dai Q, Li S, Jia X, Hejtmancik JF, Zhang Q. Guo X, et al. J Hum Genet. 2006;51(8):695-700. doi: 10.1007/s10038-006-0009-1. Epub 2006 Jul 11. J Hum Genet. 2006. PMID: 16832577

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